Patent Application
20080269191
The present invention relates to methods, compounds, and compositions for treating or preventing diseases associated with nonsense mutations in an mRNA by administering the compounds or compositions of the present invention. More particularly, the present invention relates to methods, compounds, and compositions for suppressing premature translation termination associated with a nonsense mutation in an mRNA.
Gene expression in cells depends upon the sequential processes of transcription and translation. Together, these processes produce a protein from the nucleotide sequence of its corresponding gene.
Transcription involves the synthesis of mRNA from DNA by RNA polymerase. Transcription begins at a promoter region of the gene and continues until termination is induced, such as by the formation of a stem-loop structure in the nascent RNA or the binding of the rho gene product.
Protein is then produced from mRNA by the process of translation, occurring on the ribosome with the aid of tRNA, tRNA synthetases and various other protein and RNA species. Translation comprises the three phases of initiation, elongation and termination. Translation is initiated by the formation of an initiation complex consisting of protein factors, mRNA, tRNA, cofactors and the ribosomal subunits that recognize signals on the mRNA that direct the translation machinery to begin translation on the mRNA. Once the initiation complex is formed, growth of the polypeptide chain occurs by the repetitive addition of amino acids by the peptidyl transferase activity of the ribosome as well as tRNA and tRNA synthetases. The presence of one of the three termination codons (UAA, UAG, UGA) in the A site of the ribosome signals the polypeptide chain release factors (RFs) to bind and recognize the termination signal. Subsequently, the ester bond between the 3′ nucleotide of the tRNA located in the ribosome's P site and the nascent polypeptide chain is hydrolyzed, the completed polypeptide chain is released, and the ribosome subunits are recycled for another round of translation.
Mutations of the DNA sequence in which the number of bases is altered are categorized as insertion or deletion mutations (frameshift mutations) and can result in major disruptions of the genome. Mutations of the DNA that change one base into another and result in an amino acid substitution are labeled missense mutations. Base substitutions are subdivided into the classes of transitions (one purine to another purine, or one pyrimidine to another pyrimidine) and transversions (a purine to a pyrimidine, or a pyrimidine to a purine).
Transition and transversion mutations can result in a nonsense mutation changing an amino acid codon into one of the three stop codons. These premature stop codons can produce aberrant proteins in cells as a result of premature translation termination. A nonsense mutation in an essential gene can be lethal and can also result in a number of human diseases, such as, cancers, lysosomal storage disorders, the muscular dystrophies, cystic fibrosis and hemophilia, to name a few.
The human p53 gene is the most commonly mutated gene in human cancer (Zambetti, G. P. and Levine, A., FASEB 7:855-865 (1993)). Found in both genetic and spontaneous cancers, over 50 different types of human cancers contain p53 mutations and mutations of this gene occur in 50-55% of all human cancers (Hollstein, M., et al., Nucleic Acids Res. 22:3551-55 (1994); International Agency for Research on Cancer (IARC) database). Approximately 70% of colorectal cancer, 50% of lung cancer and 40% of breast cancers contain mutant p53 (Koshland, D., Science 262:1953 (1993)). Aberrant forms of p53 are associated with poor prognosis, more aggressive tumors, metastasis, and lower 5 year survival rates (Id.). p53's role in the induction of cell growth arrest and/or apoptosis upon DNA damage is believed to be essential for the destruction of mutated cells that would have otherwise gained a growth advantage. In addition, p53 sensitizes rapidly dividing cells to apoptotic signals. Of greater than 15,000 reported mutations in the p53 gene, approximately 7% are nonsense mutations. Accordingly, there is a need for a safe and effective treatment directed to p53 nonsense mutations.
In bacterial and eukaryotic strains with nonsense mutations, suppression of the nonsense mutation can arise as a result of a mutation in one of the tRNA molecules so that the mutant tRNA can recognize the nonsense codon, as a result of mutations in proteins that are involved in the translation process, as a result of mutations in the ribosome (either the ribosomal RNA or ribosomal proteins), or by the addition of compounds known to alter the translation process (for example, cycloheximide or the aminoglycoside antibiotics). The result is that an amino acid will be incorporated into the polypeptide chain, at the site of the nonsense mutation, and translation will not prematurely terminate at the nonsense codon. The inserted amino acid will not necessarily be identical to the original amino acid of the wild-type protein, however, many amino acid substitutions do not have a gross effect on protein structure or function. Thus, a protein produced by the suppression of a nonsense mutation would be likely to possess activity close to that of the wild-type protein. This scenario provides an opportunity to treat diseases associated with nonsense mutations by avoiding premature termination of translation through suppression of the nonsense mutation.
The ability of aminoglycoside antibiotics to promote read-through of eukaryotic stop codons has attracted interest in these drugs as potential therapeutic agents in human diseases caused by nonsense mutations. One disease for which such a therapeutic strategy may be viable is classical late infantile neuronal ceroid lipofuscinosis (LINCL), a fatal childhood neurodegenerative disease with currently no effective treatment. Premature stop codon mutations in the gene CLN2 encoding the lysosomal tripeptidyl-peptidase 1 (TPP-I) are associated with disease in approximately half of children diagnosed with LINCL. The ability of the aminoglycoside gentamicin to restore TPP-I activity in LINCL cell lines has been examined. In one patient-derived cell line that was compound heterozygous for a commonly seen nonsense mutation (Arg208Stop) and a different rare nonsense mutation, approximately 7% of normal levels of TPP-I were maximally restored with gentamicin treatment. These results suggest that pharmacological suppression of nonsense mutations by aminoglycosides or functionally similar pharmaceuticals may have therapeutic potential in LINCL (Sleat et. al., Eur. J. Ped. Neurol. 5:Suppl A 57-62 (2001)).
In cultured cells having premature stop codons in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene, treatment with aminoglycosides led to the production of full-length CFTR (Bedwell et. al., Nat. Med. 3:1280-1284 (1997); Howard et. al. Nat. Med. 2: 467-469 (1996)). In mouse models for Duchenne muscular dystrophy, gentamicin sulfate was observed to suppress translational termination at premature stop codons resulting in full-length dystrophin (Barton-Davis et. al., J. Clin. Invest. 104:375-381 (1999)). A small increase in the amount of full-length dystrophin provided protection against contraction-induced damage in the mdx mice. The amino acid inserted at the site of the nonsense codon was not determined in these studies.
Accordingly, small molecule therapeutics or prophylactics that suppress premature translation termination by mediating the misreading of the nonsense codon would be useful for the treatment of a number of diseases. The discovery of small molecule drugs, particularly orally bioavailable drugs, can lead to the introduction of a broad spectrum of selective therapeutics or prophylactics to the public which can be used against disease caused by nonsense mutations is just beginning.
Clitocine (6-Amino-5-nitro-4-(β-D-ribo-furanosylamino)pyrimidine) is a naturally occurring exocyclic amino nucleoside that was first isolated from the mushroom Clitocybe inversa (Kubo et al., Tet. Lett. 27: 4277 (1986)). The total synthesis of clitocine has also been reported. (Moss et al., J. Med. Chem. 31:786-790 (1988) and Kamikawa et al., J. Chem. Soc. Chem. Commun. 195 (1988)). Clitocine has been reported to possess insecticidal activity and cytostatic activity against leukemia cell lines (Kubo et al., Tet. Lett. 27: 4277 (1986) and Moss et al., J. Med. Chem. 31:786-790 (1988)). However, the use of clitocine as a therapeutic for diseases associated with a nonsense mutation has not been disclosed until now. Nor has anyone reported the development of an analogue or derivative of clitocine that has utility as a therapeutic for cancer or a disease associated with a nonsense mutation.
Thus, there remains a need to develop characterize and optimize lead molecules for the development of novel drugs for treating or preventing diseases associated with nonsense mutations of mRNA. Accordingly, it is an object of the present invention to provide such compounds.
All documents referred to herein are incorporated by reference into the present application as though fully set forth herein.
In accordance with the present invention, compounds that suppress premature translation termination associated with a nonsense mutation in mRNA have been identified, and methods for their use provided.
In an embodiment of the invention, the present invention provides compounds of Formula (1) which are useful for suppressing premature translation termination associated with a nonsense mutation in mRNA, and for treating diseases associated with nonsense mutations in mRNA:
wherein:
Y and Z are independently selected from N or C;
W is N or CH;
n is 0, 1, 2 or 3;
R1 is hydrogen, a C6 to C8 aryl which is optionally substituted with a carboxy group, or R1 is absent when Z is N;
R2 is hydrogen; a C6 to C8 aryl which is optionally substituted with one, two, or three independently selected Ra groups; a four to seven membered heterocycle which is optionally substituted with one or more independently selected C1-C6 alkyl groups or a three to seven membered heterocycle; or R2 is absent when Y is N;
R is independently selected from a halogen; a carboxy group; a C1-C6 alkyl group optionally substituted with a four to seven membered heterocycle, a C6-C8 aryloxy group, or an amino group, wherein the four to seven membered heterocycle, C6-C8 aryloxy group, and amino group are optionally substituted with one or two independently selected C1-C6 alkyl or C6-C8 aryl groups which C6-C8 aryl groups are optionally and independently substituted with one or more C1-C6 alkyl groups; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, oxy, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a C6-C8 aryl, or a nine to ten membered heterocycle having two ring structures; a carbonyl group substituted with a five to six membered heterocycle group; a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; a nine to ten membered heterocycle having two ring structures; or two R groups, wherein R may also include an oxy group, together with the hetero-bicycle to which they are attached form a twelve to thirteen membered heterocycle having three ring structures;
wherein Ra is a halogen; a C1-C6 alkyl; a C1-C6 alkoxy which is optionally substituted with one or more independently selected halogen groups; a C6-C8 aryl; a four to seven membered heterocycle which is optionally substituted with one or more independently selected oxo groups; a carbonyl which is optionally substituted with a hydroxy or a C1-C6 alkoxy group; a carbamoyl; an amino which is optionally substituted with an independently selected C1-C6 alkyl group, wherein the C1-C6 alkyl group is optionally substituted with one or more independently selected halogens or hydroxyl groups; or two Ra groups, wherein Ra may also include an oxy group, together with the C6 to C8 aryl group to which they are attached form a nine to ten membered heterocycle having two ring structures, wherein the nine to ten membered heterocycle having two ring structures is optionally substituted with one or more independently selected halogens;
or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph of said compound of Formula 1.
In another embodiment of the invention, compounds of Formula (2) are provided which are useful for suppressing premature translation termination associated with a nonsense mutation in mRNA, and for treating diseases associated with nonsense mutations in mRNA:
wherein:
Y and Z are independently selected from N or C;
W is N or CH;
n is 0, 1, 2 or 3;
R1 is hydrogen, a C6 to C8 aryl which is optionally substituted with a carboxy group, or R1 is absent when Z is N;
R2 is hydrogen; a C6 to C8 aryl which is optionally substituted with one, two, or three independently selected Ra groups; a four to seven membered heterocycle which is optionally substituted with one or more independently selected C1-C6 alkyl groups or a three to seven membered heterocycle; or R2 is absent when Y is N;
R is independently selected from a halogen; a carboxy group; a C1-C6 alkyl group optionally substituted with a four to seven membered heterocycle, a C6-C8 aryloxy group, or an amino group, wherein the four to seven membered heterocycle, C6-C8 aryloxy group, and amino group are optionally substituted with one or two independently selected C1-C6 alkyl or C6-C8 aryl groups which C6-C8 aryl groups are optionally and independently substituted with one or more C1-C6 alkyl groups; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, oxy, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a C6-C8 aryl, or a nine to ten membered heterocycle having two ring structures; a carbonyl group substituted with a five to six membered heterocycle group; a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; a nine to ten membered heterocycle having two ring structures; or two R groups, wherein R may also include an oxy group, together with the hetero-bicycle to which they are attached form a twelve to thirteen membered heterocycle having three ring structures;
wherein Ra is a hydroxy group; a halogen; a C1-C6 alkyl which is optionally substituted with one or more independently selected halogen or hydroxy groups; a C1-C6 alkoxy which is optionally substituted with one or more independently selected halogen or phenyl groups; a C4-C8 cycloalkyl which is optionally substituted with one or more independently selected C1-C4 alkyl groups; an —Rb group; a —O—Rb group; a four to seven membered heterocycle which is optionally substituted with one or more independently selected C1-C4 alkyl, oxo, or —Rb groups; a nine to ten membered heterocycle having two ring structures; a carbonyl which is optionally substituted with a hydroxy, a C1-C4 alkyl, or a C1-C4 alkoxy group; a carbamoyl which is optionally substituted with one or two independently selected C1-C4 alkyl groups; a nitro group; a cyano group; a thio which is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; a sulfonyl which is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; an amino which is optionally substituted with one or two independently selected C1-C6 alkyl, sulfonyl, or carbonyl groups; wherein the C1-C6 alkyl group is optionally substituted with one or more independently selected halogens or hydroxyl groups, wherein the aminosulfonyl group is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group, and wherein the aminocarbonyl group is optionally substituted with a C1-C4 alkyl, a C1-C4 haloalkyl, a benzoxy, or an amino group which is optionally substituted with an —Rb group; or two Ra groups, wherein Ra may also include an oxy group, together with the C6 to C8 aryl group to which they are attached form a nine to ten membered heterocycle having two ring structures, wherein the nine to ten membered heterocycle having two ring structures is optionally substituted with one or more independently selected halogens;
wherein —Rb is a C6-C8 aryl which is optionally substituted with one or more groups independently selected from the following: a hydroxy, a halogen, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkoxy group, and an amino group which is optionally substituted with one or two independently selected C1-C4 alkyl groups;
or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph of said compound of Formula 2.
In a further embodiment of the invention, compounds of Formula (3) are provided which are useful for suppressing premature translation termination associated with a nonsense mutation in mRNA, and for treating diseases associated with nonsense mutations in mRNA:
wherein:
Y and Z are independently selected from N or C;
W is N or CH;
n is 0, 1, 2 or 3;
R1 is absent or a C6 to C8 aryl which is optionally substituted with a carboxy group;
R2 is absent; a C6 to C8 aryl which is optionally substituted with one, two, or three independently selected Ra groups; or a four to seven membered heterocycle which is optionally substituted with one or more C1-C4 alkyl groups, or a four to six membered heterocycle;
R is independently selected from a halogen; a carboxy group; a C1-C6 alkyl group optionally substituted with a C6-C8 aryloxy group, an imidazole group, or an amino group which is optionally substituted with one or two independently selected C1-C6 alkyl or C6-C8 aryl groups; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a phenyl, or a benzo[1,3]dioxole group; a carbonyl group optionally substituted with a five to six membered heterocycle group; a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; a nine to ten membered heterocycle having two ring structures; or two R groups together with the hetero-bicycle to which they are attached form a twelve to thirteen membered heterocycle having three ring structures;
wherein Ra is a hydroxy group; a halogen; a C1-C4 alkyl which is optionally substituted with one or more independently selected halogen or hydroxy groups; a C1-C4 alkoxy which is optionally substituted with one or more independently selected halogen or phenyl groups; a C4-C8 cycloalkyl which is optionally substituted with one or more independently selected C1-C4 alkyl groups; an —Rb group; a —O—Rb group; a four to six-membered heterocycle which is optionally substituted with one or more independently selected C1-C4 alkyl, oxo, or —Rb groups; a nine to ten membered heterocycle having two ring structures; a carbonyl which is optionally substituted with a hydroxy, a C1-C4 alkyl, or a C1-C4 alkoxy group; a carbamoyl which is optionally substituted with one or two C1-C4 alkyl groups; a nitro group; a cyano group; a thio which is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; a sulfonyl which is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; an amino which is optionally substituted with one or two independently selected C1-C4 alkyl, sulfonyl, or carbonyl groups; wherein the aminosulfonyl group is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; and wherein the aminocarbonyl group is optionally substituted with a C1-C4 alkyl, a C1-C4 haloalkyl, a benzoxy, or an amino group which is optionally substituted with an —Rb group, or two Ra groups together with the phenyl ring to which they are attached form a benzo[1,3]dioxole optionally substituted with one or more halogens or a 2,3-dihydro-benzofuran group;
wherein —Rb is a C6-C8 aryl which is optionally substituted with one or more of the following: a hydroxy, a halogen, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkoxy group, or an amino group which is optionally substituted with one or more C1-C4 alkyl groups;
or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph of said compound of Formula 3.
In another aspect of the invention, methods are provided for the suppression of premature translation termination associated with a nonsense mutation, and for the prevention or treatment of diseases associated with nonsense mutations of mRNA. Such diseases include, but are not limited to, genetic diseases caused by premature translation termination associated with a nonsense mutation, such as a CNS disease, an inflammatory disease, a neurodegenerative disease, an autoimmune disease, a cardiovascular disease, or a pulmonary disease; more preferably the disease is cancer (or other proliferative diseases), amyloidosis, Alzheimer's disease, atherosclerosis, giantism, dwarfism, hypothyroidism, hyperthyroidism, cystic fibrosis, aging, obesity, Parkinson's disease, Niemann Pick's disease, familial hypercholesterolemia, retinitis pigmentosa, Marfan syndrome, lysosomal storage disorders, the muscular dystrophies, cystic fibrosis, hemophilia, or classical late infantile neuronal ceroid lipofuscinosis (LINCL).
In one embodiment, the invention is directed to methods for suppressing premature translation termination associated with a nonsense mutation in mRNA comprising administering a nonsense-suppressing amount of at least one compound of the invention to a subject in need thereof.
In yet another embodiment, methods for treating cancer, lysosomal storage disorders, a muscular dystrophy, cystic fibrosis, hemophilia, or classical late infantile neuronal ceroid lipofuscinosis are provided comprising administering a therapeutically effective amount of at least one compound of the invention to a subject in need thereof.
These and other aspects of the invention will be more clearly understood with reference to the following embodiments, detailed description, and claims.
1. A method of treating or preventing a disease resulting from a somatic mutation comprising administering to a patient in need thereof an effective amount of a compound of Formula 3:
wherein:
Y and Z are independently selected from N or C;
W is N or CH;
n is 0, 1, 2 or 3;
R1 is absent or a C6 to C8 aryl which is optionally substituted with a carboxy group;
R2 is absent; a C6 to C8 aryl which is optionally substituted with one, two, or three independently selected Ra groups; or a four to seven membered heterocycle which is optionally substituted with one or more C1-C4 alkyl groups, or a four to six membered heterocycle;
R is independently selected from a halogen; a carboxy group; a C1-C6 alkyl group optionally substituted with a C6-C8 aryloxy group, an imidazole group, or an amino group which is optionally substituted with one or two independently selected C1-C6 alkyl or C6-C8 aryl groups; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a phenyl, or a benzo[1,3]dioxole group; a carbonyl group optionally substituted with a five to six membered heterocycle group; a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; a nine to ten membered heterocycle having two ring structures; or two R groups together with the hetero-bicycle to which they are attached form a twelve to thirteen membered heterocycle having three ring structures;
wherein Ra is a hydroxy group; a halogen; a C1-C4 alkyl which is optionally substituted with one or more independently selected halogen or hydroxy groups; a C1-C4 alkoxy which is optionally substituted with one or more independently selected halogen or phenyl groups; a C4-C8 cycloalkyl which is optionally substituted with one or more independently selected C1-C4 alkyl groups; an —Rb group; a —O—Rb group; a four to six-membered heterocycle which is optionally substituted with one or more independently selected C1-C4 alkyl, oxo, or —Rb groups; a nine to ten membered heterocycle having two ring structures; a carbonyl which is optionally substituted with a hydroxy, a C1-C4 alkyl, or a C1-C4 alkoxy group; a carbamoyl which is optionally substituted with one or two C1-C4 alkyl groups; a nitro group; a cyano group; a thio which is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; a sulfonyl which is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; an amino which is optionally substituted with one or two independently selected C1-C4 alkyl, sulfonyl, or carbonyl groups; wherein the aminosulfonyl group is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; and wherein the aminocarbonyl group is optionally substituted with a C1-C4 alkyl, a C1-C4 haloalkyl, a benzoxy, or an amino group which is optionally substituted with an —Rb group, or two Ra groups together with the phenyl ring to which they are attached form a benzo[1,3]dioxole optionally substituted with one or more halogens or a 2,3-dihydro-benzofuran group;
wherein —Rb is a C6-C8 aryl which is optionally substituted with one or more of the following: a hydroxy, a halogen, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkoxy group, or an amino group which is optionally substituted with one or more C1-C4 alkyl groups;
or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph of said compound of Formula 3.
2. The method of embodiment 1, wherein the compound, or a pharmaceutically acceptable salt, hydrate, solvate, clathrate or stereoisomer thereof, is administered as a composition comprising the compound and a pharmaceutically acceptable carrier or diluent.
3. The method of embodiment 1 wherein the administration is intravenous.
4. The method of embodiment 1, wherein Ra is independently selected from: a halogen; a C1 to C6 alkyl; a C1 to C6 haloalkyl; a C1 to C6 alkoxy; a C1 to C6 haloalkoxy; a C6 to C8 aryl group; a carboxy group; a carbamoyl group; an amino group which is optionally substituted with one or two independently selected hydroxy groups, halogens, C1 to C6 alkyls, or C1 to C6 haloalkyls; or a four to six membered heterocycle optionally substituted with an oxo group.
5. The method of embodiment 1, wherein the four to seven membered heterocycle is selected from an azetidine group, a pyrrolidine group, a piperidine group, a piperazine group, a morpholine group, a [1,4]diazepane group, a pyrazole group, an imidazole group, a [1,2,4] triazole group, a pyridine group, a furan group, and a thiophene group.
6. The method of embodiment 1, wherein the nine to ten membered heterocycle having two ring structures is selected from a benzofuran group, a 2,3-dihydro-benzofuran group, a benzo[1,3]dioxole group, a 2,3-dihydro-isoindole group, a 2,3-dihydro-indole group, a 1,2,3,4-tetrahydro-isoquinoline group, and a 1,4-dioxa-8-aza-spiro[4.5]decane group.
7. The method of embodiment 1, wherein R2 is selected from the following, wherein the * indicates the bond of attachment:
8. The method of embodiment 1, wherein R is selected from the following, wherein the * indicates the bond of attachment:
9. The method of embodiment 1, wherein said compound of Formula 3 is a compound of Formula 3-A:
10. The method of embodiment 9, wherein n is 1 and R is a carboxy group.
11. The method of embodiment 9, wherein n is 1 and the R group is in the 5 or 6 position.
12. The method of embodiment 9, wherein R2 is a C6 to C8 aryl, optionally substituted with one, two, or three —Ra groups, wherein Ra is independently selected from: a halogen; a C1 to C6 alkyl; a C1 to C6 haloalkyl; a C1 to C6 alkoxy; a C1 to C6 haloalkoxy; a C6 to C8 aryl group; a carboxy group; a carbamoyl group; an amino group which is optionally substituted with one or two independently selected hydroxy groups, halogens, C1 to C6 alkyls, or C1 to C6 haloalkyls; or a four to six membered heterocycle optionally substituted with an oxo group.
13. The method of embodiment 9, wherein R2 is a phenyl group optionally substituted with a carboxy group.
14. The method of embodiment 1, wherein said compound of Formula 3 is a compound of Formula 3-B:
15. The method of embodiment 14, wherein R1 is a phenyl group optionally substituted with a carboxy group.
16. The method of embodiment 14, wherein R is a C1-C6 alkyl; a C1-C6 alkoxy; a C6-C8 aryl optionally substituted with one or more halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; or two R groups together with the hetero-bicycle to which they are attached form a twelve to thirteen membered heterocycle having three ring structures.
17. The method of embodiment 16, wherein the twelve to thirteen membered heterocycle is selected from the following, wherein the * indicates the bond of attachment to R1:
18. A method of treating or preventing a disease resulting from a somatic mutation comprising administering to a patient in need thereof an effective amount of a compound of Formula 4:
wherein:
Y and Z are independently selected from N or C;
W is N or CH;
R1 is absent or a C6 to C8 aryl which is optionally substituted with a carboxy group;
R2 is absent; a C6 to C8 aryl which is optionally substituted with one, two, or three independently selected —Ra groups; or a four to seven membered heterocycle which is optionally substituted with one or more independently selected C1-C4 alkyl groups, or a four to six membered heterocycle;
R3 is hydrogen, a halogen, a carboxy group, or R3 together with R4 and the heterocycle to which they are attached preferably form a twelve to thirteen membered heterocycle with three ring structures;
R4 is hydrogen, a halogen; a carboxy group; a C1-C6 alkyl group; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a phenyl, or a benzo[1,3]dioxole group; a carbonyl group substituted with a five to six membered heterocycle group; or a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; a nine to ten membered heterocycle having two ring structures; or R3 together with R4 and the heterocycle to which they are attached preferably form a twelve to thirteen membered heterocycle with three ring structures;
R5 is independently selected from: hydrogen, a halogen; a carboxy group; a C1-C6 alkyl group optionally substituted with a C6-C8 aryloxy group, an imidazole group, or an amino group which is optionally substituted with one or two independently selected C1-C6 alkyl or C6-C8 aryl groups; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; a carbonyl group substituted with a five to six membered heterocycle group; a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; or a nine to ten membered heterocycle having two ring structures;
or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph of said compound of Formula 4.
19. The method of embodiment 18, wherein R4 is selected from:
20. The method of embodiment 18, wherein R5 is selected from the following, wherein the * indicates the bond of attachment:
21. The method of claim 18, wherein said compound of Formula 4 is a compound of Formula 4-A:
22. The method of embodiment 21, wherein R2 is a C6 to C8 aryl, optionally substituted with one, two, or three —Ra groups, wherein Ra is independently selected from: a halogen; a C1 to C6 alkyl; a C1 to C6 haloalkyl; a C1 to C6 alkoxy; a C1 to C6 haloalkoxy; a C6 to C8 aryl group; a carboxy group; a carbamoyl group; an amino group which is optionally substituted with one or two independently selected hydroxy groups, halogens, C1 to C6 alkyls, or C1 to C6 haloalkyls; or a four to six membered heterocycle optionally substituted with an oxo group.
23. The method of embodiment 18, wherein said compound of Formula 4 is a compound of Formula 4-B:
24. The method of embodiment 23, wherein R1 is a phenyl group optionally substituted with a carboxy group.
25. A method of treating or preventing an autoimmune disease, a blood disease, a collagen disease, diabetes, a neurodegenerative disease, a cardiovascular disease, a pulmonary disease, or an inflammatory disease or central nervous system disease comprising administering to a patient in need thereof an effective amount of a compound of Formula 3 or 4, or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph thereof
26. The method of embodiment 25, wherein the administration is intravenous.
27. The method of embodiment 25, wherein the autoimmune disease is rheumatoid arthritis or graft versus host disease.
28. The method of embodiment 25, wherein the inflammatory disease is arthritis.
29. The method of embodiment 25, wherein the central nervous system disease is multiple sclerosis, muscular dystrophy, Duchenne muscular dystrophy, Alzheimer's disease, a neurodegenerative disease or Parkinson's disease.
30. The method of embodiment 25, wherein the blood disorder is hemophilia, Von Willebrand disease, ataxia-telangiectasia, β-thalassemia or kidney stones.
31. The method of embodiment 25, wherein the collagen disease is osteogenesis imperfecta or cirrhosis.
32. A method of treating or preventing familial polycythemia, immunodeficiency, kidney disease, muscular dystrophy, heart disease, kidney stones, ataxia-telangiectasia, cystic fibrosis, familial hypercholesterolemia, retinitis pigmentosa, amyloidosis, hemophilia, Alzheimer's disease, Tay Sachs disease, Niemann Pick disease, Parkinson's disease, atherosclerosis, giantism, dwarfism, hyperthyroidism, aging, obesity, Duchenne muscular dystrophy, epidermolysis bullosa or Marfan syndrome comprising administering to a patient in need thereof an effective amount of a compound of Formula 3 or 4, or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph thereof.
33. The method of embodiment 32, wherein the administration is intravenous.
34. A method of treating or preventing cancer in a human comprising administering to a human in need thereof an effective amount of a compound of Formula 3, or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph thereof.
35. The method of embodiment 34, wherein the administration is intravenous.
36. The method of embodiment 34, wherein the cancer is of the head and neck, eye, skin, mouth, throat, esophagus, chest, bone, blood, lung, colon, sigmoid, rectum, stomach, prostate, breast, ovaries, kidney, liver, pancreas, brain, intestine, heart or adrenals.
37. The method of embodiment 34, wherein the compound, or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph thereof, comprises a pharmaceutically acceptable carrier or diluent.
38. The method of embodiment 34, wherein the cancer is a solid tumor.
39. The method of embodiment 34, wherein the cancer is sarcoma, carcinoma, fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, pancreatic cancer, breast cancer, ovarian cancer, prostate cancer, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilms' tumor, cervical cancer, testicular tumor, lung carcinoma, small cell lung carcinoma, bladder carcinoma, epithelial carcinoma, glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, Kaposi's sarcoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, menangioma, melanoma, neuroblastoma, retinoblastoma, a blood-born tumor or multiple myeloma.
40. The method of embodiment 34, wherein the cancer is acute lymphoblastic leukemia, acute lymphoblastic B-cell leukemia, acute lymphoblastic T-cell leukemia, acute myeloblastic leukemia, acute promyelocytic leukemia, acute monoblastic leukemia, acute erythroleukemic leukemia, acute megakaryoblastic leukemia, acute myelomonocytic leukemia, acute nonlymphocyctic leukemia, acute undifferentiated leukemia, chronic myelocytic leukemia, chronic lymphocytic leukemia, hairy cell leukemia, or multiple myeloma.
41. A method of treating or preventing a disease associated with a mutation of the p53 gene comprising administering to a patient in need thereof an effective amount of a compound of Formula 3 or 4, or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph thereof.
42. The method of embodiment 41, wherein the administration is intravenous.
43. The method of embodiment 41, wherein the disease is sarcoma, carcinomas, fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, pancreatic cancer, breast cancer, ovarian cancer, prostate cancer, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilms' tumor, cervical cancer, testicular tumor, lung carcinoma, small cell lung carcinoma, bladder carcinoma, epithelial carcinoma, glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, Kaposi's sarcoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, menangioma, melanoma, neuroblastoma or retinoblastoma.
44. A method of inhibiting the growth of a cancer cell comprising contacting the cancer cell with an effective amount of a compound of Formula 3 or 4, or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph thereof.
45. A method for selectively producing a protein in a mammal comprising transcribing a gene containing a nonsense mutation in the mammal; and providing an effective amount of a compound of the present invention to said mammal, wherein said protein is produced by said mammal.
Premature translation termination can produce aberrant proteins which can be lethal or can cause a number of diseases, including as non-limiting examples, cancers, lysosomal storage disorders, the muscular dystrophies, cystic fibrosis and hemophilia. In accordance with the present invention, compounds that suppress nonsense mutations have been identified, and methods for their use provided.
A. Compounds of the Invention
In one aspect of the invention, compounds of the invention are provided which are useful in suppression of a nonsense mutation. Compounds of the present invention are also useful for increasing the expression of a protein. In certain embodiments, the compounds of the invention specifically suppresses a nonsense mutation, while in other embodiments, the compounds of the invention suppress a nonsense mutation as well as treat a disease, including as non-limiting examples, cancers, lysosomal storage disorders, the muscular dystrophies, cystic fibrosis and hemophilia.
In an embodiment of the invention, the present invention provides compounds of Formula (1) which are useful for suppressing premature translation termination associated with a nonsense mutation in mRNA, and for treating diseases associated with nonsense mutations in mRNA:
wherein:
Y and Z are independently selected from N or C;
W is N or CH;
n is 0, 1, 2 or 3;
R1 is hydrogen, a C6 to C8 aryl which is optionally substituted with a carboxy group, or R1 is absent when Z is N;
R2 is hydrogen; a C6 to C8 aryl which is optionally substituted with one, two, or three independently selected Ra groups; a four to seven membered heterocycle which is optionally substituted with one or more independently selected C1-C6 alkyl groups or a three to seven membered heterocycle; or R2 is absent when Y is N;
R is independently selected from a halogen; a carboxy group; a C1-C6 alkyl group optionally substituted with a four to seven membered heterocycle, a C6-C8 aryloxy group, or an amino group, wherein the four to seven membered heterocycle, C6-C8 aryloxy group, and amino group are optionally substituted with one or two independently selected C1-C6 alkyl or C6-C8 aryl groups which C6-C8 aryl groups are optionally and independently substituted with one or more C1-C6 alkyl groups; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, oxy, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a C6-C8 aryl, or a nine to ten membered heterocycle having two ring structures; a carbonyl group substituted with a five to six membered heterocycle group; a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; a nine to ten membered heterocycle having two ring structures; or two R groups, wherein R may also include an oxy group, together with the hetero-bicycle to which they are attached form a twelve to thirteen membered heterocycle having three ring structures;
wherein Ra is a halogen; a C1-C6 alkyl; a C1-C6 alkoxy which is optionally substituted with one or more independently selected halogen groups; a C6-C8 aryl; a four to seven membered heterocycle which is optionally substituted with one or more independently selected oxo groups; a carbonyl which is optionally substituted with a hydroxy or a C1-C6 alkoxy group; a carbamoyl; an amino which is optionally substituted with an independently selected C1-C6 alkyl group, wherein the C1-C6 alkyl group is optionally substituted with one or more independently selected halogens or hydroxyl groups; or two Ra groups, wherein Ra may also include an oxy group, together with the C6 to C8 aryl group to which they are attached form a nine to ten membered heterocycle having two ring structures, wherein the nine to ten membered heterocycle having two ring structures is optionally substituted with one or more independently selected halogens;
or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph of said compound of Formula 1.
In another embodiment of the invention, compounds of Formula (2) are provided which are useful for suppressing premature translation termination associated with a nonsense mutation in mRNA, and for treating diseases associated with nonsense mutations in mRNA:
wherein:
Y and Z are independently selected from N or C;
W is N or CH;
n is 0, 1, 2 or 3;
R1 is hydrogen, a C6 to C8 aryl which is optionally substituted with a carboxy group, or R1 is absent when Z is N;
R2 is hydrogen; a C6 to C8 aryl which is optionally substituted with one, two, or three independently selected Ra groups; a four to seven membered heterocycle which is optionally substituted with one or more independently selected C1-C6 alkyl groups or a three to seven membered heterocycle; or R2 is absent when Y is N;
R is independently selected from a halogen; a carboxy group; a C1-C6 alkyl group optionally substituted with a four to seven membered heterocycle, a C6-C8 aryloxy group, or an amino group, wherein the four to seven membered heterocycle, C6-C8 aryloxy group, and amino group are optionally substituted with one or two independently selected C1-C6 alkyl or C6-C8 aryl groups which C6-C8 aryl groups are optionally and independently substituted with one or more C1-C6 alkyl groups; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, OXY, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a C6-C8 aryl, or a nine to ten membered heterocycle having two ring structures; a carbonyl group substituted with a five to six membered heterocycle group; a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; a nine to ten membered heterocycle having two ring structures; or two R groups, wherein R may also include an oxy group, together with the hetero-bicycle to which they are attached form a twelve to thirteen membered heterocycle having three ring structures;
wherein Ra is a hydroxy group; a halogen; a C1-C6 alkyl which is optionally substituted with one or more independently selected halogen or hydroxy groups; a C1-C6 alkoxy which is optionally substituted with one or more independently selected halogen or phenyl groups; a C4-C8 cycloalkyl which is optionally substituted with one or more independently selected C1-C4 alkyl groups; an —Rb group; a —O—Rb group; a four to seven membered heterocycle which is optionally substituted with one or more independently selected C1-C4 alkyl, oxo, or —Rb groups; a nine to ten membered heterocycle having two ring structures; a carbonyl which is optionally substituted with a hydroxy, a C1-C4 alkyl, or a C1-C4 alkoxy group; a carbamoyl which is optionally substituted with one or two independently selected C1-C4 alkyl groups; a nitro group; a cyano group; a thio which is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; a sulfonyl which is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; an amino which is optionally substituted with one or two independently selected C1-C6 alkyl, sulfonyl, or carbonyl groups; wherein the C1-C6 alkyl group is optionally substituted with one or more independently selected halogens or hydroxyl groups, wherein the aminosulfonyl group is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group, and wherein the aminocarbonyl group is optionally substituted with a C1-C4 alkyl, a C1-C4 haloalkyl, a benzoxy, or an amino group which is optionally substituted with an —Rb group; or two Ra groups, wherein Ra may also include an oxy group, together with the C6 to C8 aryl to which they are attached form a nine to ten membered heterocycle having two ring structures, wherein the nine to ten membered heterocycle having two ring structures is optionally substituted with one or more independently selected halogens;
wherein —Rb is a C6-C8 aryl which is optionally substituted with one or more groups independently selected from the following: a hydroxy, a halogen, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkoxy group, and an amino group which is optionally substituted with one or two independently selected C1-C4 alkyl groups;
or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph of said compound of Formula 2.
In a further embodiment of the invention, compounds of Formula (3) are provided which are useful for suppressing premature translation termination associated with a nonsense mutation in mRNA, and for treating diseases associated with nonsense mutations in mRNA:
wherein:
Y and Z are independently selected from N or C;
W is N or CH;
n is 0, 1, 2 or 3;
R1 is absent or a C6 to C8 aryl which is optionally substituted with a carboxy group;
R2 is absent; a C6 to C8 aryl which is optionally substituted with one, two, or three independently selected Ra groups; or a four to seven membered heterocycle which is optionally substituted with one or more C1-C4 alkyl groups, or a four to six membered heterocycle;
R is independently selected from a halogen; a carboxy group; a C1-C6 alkyl group optionally substituted with a C6-C8 aryloxy group, an imidazole group, or an amino group which is optionally substituted with one or two independently selected C1-C6 alkyl or C6-C8 aryl groups; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a phenyl, or a benzo[1,3]dioxole group; a carbonyl group substituted with a five to six membered heterocycle group; a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; a nine to ten membered heterocycle having two ring structures; or two R groups together with the hetero-bicycle to which they are attached form a twelve to thirteen membered heterocycle having three ring structures;
wherein Ra is a hydroxy group; a halogen; a C1-C4 alkyl which is optionally substituted with one or more independently selected halogen or hydroxy groups; a C1-C4 alkoxy which is optionally substituted with one or more independently selected halogen or phenyl groups; a C4-C8 cycloalkyl which is optionally substituted with one or more independently selected C1-C4 alkyl groups; an —Rb group; a —O—Rb group; a four to six-membered heterocycle which is optionally substituted with one or more independently selected C1-C4 alkyl, oxo, or —Rb groups; a nine to ten membered heterocycle having two ring structures; a carbonyl which is optionally substituted with a hydroxy, a C1-C4 alkyl, or a C1-C4 alkoxy group; a carbamoyl which is optionally substituted with one or two C1-C4 alkyl groups; a nitro group; a cyano group; a thio which is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; a sulfonyl which is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; an amino which is optionally substituted with one or two independently selected C1-C4 alkyl, sulfonyl, or carbonyl groups; wherein the aminosulfonyl group is optionally substituted with a hydroxy, a C1-C4 alkyl, or —Rb group; and wherein the aminocarbonyl group is optionally substituted with a C1-C4 alkyl, a C1-C4 haloalkyl, a benzoxy, or an amino group which is optionally substituted with an —Rb group, or two Ra groups together with the phenyl ring to which they are attached form a benzo[1,3]dioxole optionally substituted with one or more halogens or a 2,3-dihydro-benzofuran group;
wherein —Rb is a C6-C8 aryl which is optionally substituted with one or more of the following: a hydroxy, a halogen, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkoxy group, or an amino group which is optionally substituted with one or more C1-C4 alkyl groups;
or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph of said compound of Formula 3.
In an embodiment of Formula 1, a compound of Formula 1 is provided with the proviso that at least one of R1 and R2 is not hydrogen. In embodiments of Formulas 1A and 1B, compounds of Formulas 1A and 1B are provided with the proviso that at least one of R1 and R2 is not hydrogen.
In an embodiment of Formula 2, a compound of Formula 2 is provided with the proviso that at least one of R1 and R2 is not hydrogen. In embodiments of Formulas 2A and 2B, compounds of Formulas 2A and 2B are provided with the proviso that at least one of R1 and R2 is not hydrogen.
In an embodiment of Formula 4, a compound of Formula 4 is provided with the proviso that at least one of R1 and R2 is not hydrogen. In an embodiment of Formula 4A, a compound of Formula 4A is provided with the proviso that at least one of R1 and R2 is not hydrogen.
In an embodiment of Formulas 1, 2, and 3, Y is N. In another embodiment of Formulas 1, 2, and 3, Z is N. In a further embodiment of Formulas 1, 2, and 3, both Y and Z are N. In another embodiment of Formulas 1, 2, and 3, neither Y nor Z is N.
In an embodiment of Formulas 1, 2, and 3, Y is C. In another embodiment of Formula I, Z is C. In a further embodiment of Formulas 1, 2, and 3, both Y and Z are C.
In another embodiment of Formulas 1, 2, and 3, neither Y nor Z is C.
In an embodiment of Formulas 1, 2, and 3, W is CH.
In an embodiment of Formulas 1, 2, and 3, W is N.
In an embodiment of Formulas 1, 2, and 3, n is 0. In another embodiment of Formulas 1, 2, and 3, n is 1. In another embodiment of Formulas 1, 2, and 3, n is 2. In a further embodiment of Formulas 1, 2, and 3, n is 3. In a preferred embodiment of Formulas 1, 2, and 3, n is 1.
In an embodiment of Formulas 1, 2, and 3, R1 is absent. In another embodiment of Formulas 1, 2, and 3, Z is N and R1 is absent. In a further embodiment of Formulas 1, 2, and 3, Y is C, Z is N, and R1 is absent.
In another embodiment of Formulas 1, 2, and 3, R1 is C6 to C8 aryl optionally substituted with a carboxy group. In another embodiment of Formulas 1, 2, and 3, R1 is a phenyl group optionally substituted with a carboxy group. In another embodiment of Formulas 1, 2, and 3, R1 is a phenyl group substituted with a carboxy group, wherein the carboxy group is in the ortho, meta or para position. In a preferred embodiment of Formulas 1, 2, and 3, R1 is a phenyl group substituted with a carboxy group, wherein the carboxy group is in the ortho, meta or para position. In a further embodiment of Formulas 1, 2, and 3, Y is N, n is 1 or 2, and R1 is C6 to C8 aryl optionally substituted with a carboxy group. In a further embodiment of Formulas 1, 2, and 3, Y is N, n is 1 or 2, and R1 is a phenyl group optionally substituted with a carboxy group. In another embodiment of Formulas 1, 2, and 3, Y is N, n is 1, and R1 is phenyl group substituted with a carboxy group, wherein the carboxy group is in the ortho, meta or para, and preferably in the meta or para, position.
In an embodiment of Formulas 1, 2, and 3, R2 is absent. In another embodiment of Formulas 1, 2, and 3, R2 is absent and R1 is C6 to C8 aryl optionally substituted with a carboxy group. In another embodiment of Formulas 1, 2, and 3, R2 is absent and R1 is a phenyl group optionally substituted with a carboxy group. In another embodiment of Formulas 1, 2, and 3, R2 is absent and R1 is a phenyl group substituted with a carboxy group, wherein the carboxy group is in the ortho, meta or para position. In another embodiment of Formulas 1, 2, and 3, R2 is absent and R1 is a phenyl group substituted with a carboxy group, wherein the carboxy group is in the meta or para position. In a further embodiment of Formulas 1, 2, and 3, Y is N, n is 1 or 2, R2 is absent and R1 is C6 to C8 aryl optionally substituted with a carboxy group.
In an embodiment of Formulas 1, 2, and 3, R2 is C6 to C8 aryl optionally substituted with one, two, or three independently selected Ra groups. In an embodiment of Formulas 1, 2, and 3, R2 is C6 to C8 aryl optionally substituted with a carboxy group. In another embodiment of Formulas 1, 2, and 3, R2 is a phenyl group optionally substituted with a carboxy group. In another embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with a carboxy group, wherein the carboxy group is in the ortho, meta or para position. In a further embodiment of Formulas 1, 2, and 3, Z is N and R2 is C6 to C8 aryl optionally substituted with a carboxy group. In another embodiment of Formulas 1, 2, and 3, Z is N and R2 is a phenyl group optionally substituted with a carboxy group. In another embodiment of Formulas 1, 2, and 3, Z is N and R2 is a phenyl group substituted with a carboxy group, wherein the carboxy group is in the ortho, meta or para position. In a further embodiment of Formulas 1, 2, and 3, Z is N and R2 is a phenyl group substituted with a carboxy group, wherein the carboxy group is in the meta or para position.
In an embodiment of Formulas 1, 2, and 3, R2 is C6-C8 aryl optionally substituted with one, two or three independently selected Ra groups. In an embodiment of Formulas 1, 2, and 3, R2 is an unsubstituted C6-C8 aryl. In an embodiment of Formulas 1, 2, and 3, R2 is a phenyl group optionally substituted with one, two or three independently selected Ra groups. In an embodiment of Formulas 1, 2, and 3, R2 is an unsubstituted phenyl group. In an embodiment of Formulas 1 and 2, R2 is C6-C8 aryl substituted with one C1-C6 alkyl group. In an embodiment of Formula 3, R2 is C6-C8 aryl substituted with one C1-C4 alkyl group. In an embodiment of Formulas 1, 2, and 3, R2 is C6-C8 aryl substituted with one methyl group. In another embodiment of Formulas 1, 2, and 3, R2 is C6-C8 aryl substituted with one propyl group. In an embodiment of Formulas 1, 2, and 3, R2 is C6-C8 aryl substituted with one isopropyl group. In an embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one C1-C4 alkyl group. In an embodiment of Formulas 1, 2, and 3, R2 is phenyl group substituted with one methyl group. In an embodiment of Formulas 1, 2, and 3, R2 is phenyl group substituted with one propyl group. In another embodiment of Formulas 1, 2, and 3, R2 is phenyl group substituted with one isopropyl group.
In an embodiment of Formulas 1, 2, and 3, R2 is C6-C8 aryl substituted with one C6-C8 aryl group. In another embodiment of Formulas 1, 2, and 3, R2 is C6-C8 aryl substituted with one phenyl group. In an embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one C6 to C8 aryl group. In a further embodiment of Formulas 1, 2, and 3, R2 is phenyl group substituted with one phenyl group.
In an embodiment of Formulas 1 and 2, R2 is a C6-C8 aryl group substituted with one four to seven membered heterocycle, wherein the four to seven membered heterocycle is optionally substituted with an oxo group. In an embodiment of Formula 3, R2 is a C6-C8 aryl group substituted with one four to six membered heterocycle, wherein the four to six membered heterocycle is optionally substituted with an oxo group. In an embodiment of Formulas 1, 2, and 3, R2 is C6-C8 aryl substituted with one pyrrolidine group, wherein the pyrrolidine is optionally substituted with an oxo group. In another embodiment of Formulas 1, 2, and 3, R2 is C6-C8 aryl substituted with one morpholine group. In another embodiment of Formulas 1, 2, and 3, R2 is C6-C8 aryl substituted with one pyrazole group. In another embodiment of Formulas 1, 2, and 3, R2 is C6-C8 aryl substituted with one azetidine group. In an embodiment of Formulas 1 and 2, R2 is phenyl group substituted with one four to seven membered heterocycle, which four to seven membered heterocycle is optionally substituted with an oxo group. In an embodiment of Formula 3, R2 is phenyl group substituted with one four to six membered heterocycle, which four to six membered heterocycle is optionally substituted with an oxo group. In an embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one pyrrolidine group, which pyrrolidine is optionally substituted with an oxo group. In another embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one morpholine group. In another embodiment of Formulas 1, 2, and 3, R2 is phenyl group substituted with one pyrazole group. In another embodiment of Formulas 1, 2, and 3, R2 is phenyl group substituted with one azetidine group.
In an embodiment of Formulas 1, 2, and 3, R2 is a C6-C8 aryl group substituted with one halogen. In an embodiment of Formulas 1, 2, and 3, R2 is a C6-C8 aryl group substituted with one bromine. In an embodiment of Formulas 1, 2, and 3, R2 is a C6-C8 aryl group substituted with one fluorine. In an embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one halogen. In another embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one bromine. In another embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one fluorine.
In an embodiment of Formula 1, R2 is a C6-C8 aryl group substituted with one, two or three C1-C6 alkoxy groups, each of which is optionally substituted with one or more independently selected halogens. In an embodiment of Formula 2, R2 is a C6-C8 aryl group substituted with one, two or three C1-C6 alkoxy groups, each of which is optionally substituted with one or more independently selected halogen or phenyl groups. In an embodiment of Formula 3, R2 is a C6-C8 aryl group substituted with one, two or three C1-C4 alkoxy groups, each of which is optionally substituted with one or more independently selected halogen or phenyl groups. In an embodiment of Formulas 1, 2, and 3, R2 is a C6-C8 aryl group substituted with one methoxy group. In an embodiment of Formulas 1, 2, and 3, R2 is a C6-C8 aryl group substituted with one methoxy group, wherein the methoxy group is substituted with up to three independently selected halogens. In an embodiment of Formulas 1, 2, and 3, R2 is a C6-C8 aryl group substituted with a trifluoromethoxy group. In an embodiment of Formulas 1, 2, and 3, R2 is a C6-C8 aryl group substituted with two methoxy groups. In an embodiment of Formulas 1, 2, and 3, R2 is a C6-C8 aryl group substituted with two trifluoromethoxy groups.
In another embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one, two or three C1-C4 alkoxy groups. In an embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one methoxy group. In an embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one, two or three C1-C4 alkoxy groups, each of which is optionally substituted with one or more independently selected halogens. In an embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one methoxy group. In an embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with one methoxy group, which is substituted with three independently selected halogens. In an embodiment of Formulas 1, 2, and 3, R2 is a C6-C8 aryl group substituted with one trifluoromethoxy group. In an embodiment of Formulas 1, 2, and 3, R2 is a phenyl group substituted with two methoxy groups.
In an embodiment of Formulas 1 and 2, R2 is a C6-C8 aryl group substituted with an amino group, wherein the amino group is optionally substituted with a C1-C6 alkyl, which is optionally substituted with one or more independently selected halogens. In an embodiment of Formulas 1 and 2, R2 is a C6-C8 aryl group substituted with an amino group, wherein the amino group is optionally substituted with a C1-C6 alkyl, which is optionally substituted with one or more hydroxyl groups. In an embodiment of Formulas 1 and 2, R2 is a C6-C8 aryl group substituted with an amino group, wherein the amino group is substituted with a propyl group, which is optionally substituted with one or more independently selected halogens. In an embodiment of Formulas 1 and 2, R2 is a C6-C8 aryl group substituted with an amino group, wherein the amino group is substituted with a propyl group, which is optionally substituted with one chlorine. In an embodiment of Formulas 1 and 2, R2 is a C6-C8 aryl group substituted with an amino group, wherein the amino group is substituted with a propyl group, which is optionally substituted with one hydroxyl group. In an embodiment of Formulas 1 and 2, R2 is a C6-C8 aryl group substituted with an amino group, wherein the amino group is substituted with a pentyl group, which is optionally substituted with one hydroxyl group.
In an embodiment of Formulas 1 and 2, R2 is a phenyl group substituted with an amino group, wherein the amino group is optionally substituted with a C1-C6 alkyl, which is optionally substituted with one or more independently selected halogens. In an embodiment of Formulas 1 and 2, R2 is a phenyl group substituted with an amino group, wherein the amino group is optionally substituted with a C1-C6 alkyl, which is optionally substituted with one or more hydroxyl groups. In an embodiment of Formulas 1 and 2, R2 is a phenyl group substituted with an amino group, wherein the amino group is substituted with a propyl group, which is optionally substituted with one or more independently selected halogens. In an embodiment of Formulas 1 and 2, R2 is a phenyl group substituted with an amino group, wherein the amino group is substituted with a propyl group, which is optionally substituted with one chlorine. In an embodiment of Formulas 1 and 2, R2 is a phenyl group substituted with an amino group, wherein the amino group is substituted with a propyl group, which is optionally substituted with one hydroxyl group. In an embodiment of Formulas 1 and 2, R2 is a phenyl group substituted with an amino group, wherein the amino group is substituted with a pentyl group, which is optionally substituted with one hydroxyl group.
In an embodiment of Formulas 1, 2, and 3, R2 is C6 to C8 aryl optionally substituted with a carbamoyl group. In another embodiment of Formulas 1, 2, and 3, R2 is phenyl group optionally substituted with a carbamoyl group.
In an embodiment of Formulas 1, 2, and 3, R2 is C6 to C8 aryl optionally substituted with two independently selected Ra groups. In an embodiment of Formulas 1 and 2, R2 is C6 to C8 aryl substituted with two Ra groups, wherein the two Ra groups together with the C6 to C8 aryl to which they are attached form a nine to ten membered heterocycle having two ring structures, wherein the nine to ten membered heterocycle having two ring structures is optionally substituted with one or more independently selected halogens. In an embodiment of Formulas 1, 2, and 3, R2 is C6 to C8 aryl substituted with two Ra groups, wherein the two Ra groups together with the C6 to C8 aryl form a benzo[1,3]dioxole, which benzo[1,3]dioxole is optionally substituted with one or more independently selected halogens. In an embodiment of Formulas 1, 2, and 3, R2 is C6 to C8 aryl substituted with two Ra groups, wherein the two Ra groups together with the C6 to C8 aryl to which they are attached form a benzo[1,3]dioxole, wherein the benzo[1,3]dioxole is optionally substituted with two fluorines. In an embodiment of Formulas 1, 2, and 3, R2 is C6 to C8 aryl substituted with two Ra groups, wherein the two Ra groups together with the C6 to C8 aryl form a 2,3-dihydro-benzofuran.
In an embodiment of Formulas 1, 2, and 3, R2 is phenyl optionally substituted with two independently selected Ra groups. In an embodiment of Formulas 1, 2, and 3, R2 is phenyl substituted with two Ra groups, wherein the two Ra groups together with the phenyl to which they are attached form a nine to ten membered heterocycle having two ring structures, wherein the nine to ten membered heterocycle having two ring structures is optionally substituted with one or more independently selected halogens. In an embodiment of Formulas 1, 2, and 3, R2 is phenyl substituted with two Ra groups, wherein the two Ra groups together with the phenyl form a benzo[1,3]dioxole, which benzo[1,3]dioxole is optionally substituted with one or more independently selected halogens. In an embodiment of Formulas 1, 2, and 3, R2 is phenyl substituted with two Ra groups, wherein the two Ra groups together with the phenyl to which they are attached form a benzo[1,3]dioxole, wherein the benzo[1,3]dioxole is optionally substituted with two fluorines. In an embodiment of Formulas 1, 2, and 3, R2 is phenyl substituted with two Ra groups, wherein the two Ra groups together with the phenyl form a 2,3-dihydro-benzofuran.
In an embodiment of Formulas 1 and 2, R2 is a four to seven membered heterocycle, which is optionally substituted with one or more independently selected C1 to C6 alkyl groups or a three to seven membered heterocycle. In an embodiment of Formula 3, R2 is a four to seven membered heterocycle, which is optionally substituted with one or more independently selected C1 to C4 alkyl groups or a four to six membered heterocycle. In an embodiment of Formulas 1, 2, and 3, R2 is a five membered heterocycle optionally substituted with one or more independently selected alkyl groups. In an embodiment of Formulas 1, 2, and 3, R2 is a furyl group. In an embodiment of Formulas 1 and 2 R2 is a furyl group substituted with one or more independently selected C1 to C6 alkyl groups. In an embodiment of Formula 3, R2 is a furyl group substituted with one or more independently selected C1 to C4 alkyl groups. In another embodiment of Formulas 1 and 2, R2 is a thiophenyl group substituted with one or more independently selected C1 to C6 alkyl groups. In another embodiment of Formula 3, R2 is a thiophenyl group substituted with one or more independently selected C1 to C4 alkyl groups. In an embodiment of Formulas 1, 2, and 3, R2 is a furyl group substituted with two methyl groups. In another embodiment of Formulas 1, 2, and 3, R2 is a thiophenyl group substituted with a methyl group.
In another embodiment of Formulas 1 and 2, R2 is a six membered heterocycle, which is optionally substituted with a three to seven membered heterocycle. In another embodiment of Formula 3, R2 is a six membered heterocycle, which is optionally substituted with a four to six membered heterocycle. In another embodiment of Formulas 1, 2, and 3, R2 is a six membered heterocycle, which is optionally substituted with a four membered heterocycle. In another embodiment of Formulas 1, 2, and 3, R2 is a six membered heterocycle, which is optionally substituted with a five membered heterocycle. In another embodiment of Formulas 1, 2, and 3, R2 is a six membered heterocycle, which is optionally substituted with a six membered heterocycle. In an embodiment of Formulas 1, 2, and 3, R2 is a pyridine group, optionally substituted with a four to six membered heterocycle. In another embodiment of Formulas 1, 2, and 3, R2 is a six membered heterocycle, which is optionally substituted with a pyrrolidine, mophiline, piperidine, azetidine, or piperazine group. In another embodiment of Formulas 1, 2, and 3, R2 is a pyridine group, optionally substituted with a pyrrolidine group. In another embodiment of Formulas 1, 2, and 3, R2 is a pyridine group, optionally substituted with a morpholine group. In another embodiment of Formulas 1, 2, and 3, R2 is a pyridine group, optionally substituted with a piperidine group. In another embodiment of Formulas 1, 2, and 3, R2 is a pyridine group, optionally substituted with an azetidine group. In another embodiment of Formulas 1, 2, and 3, R2 is a pyridine group, optionally substituted with a piperazine group.
In an embodiment of Formulas 1, 2, and 3, R is a C1-C6 alkyl group optionally substituted with a C6-C8 aryloxy group, wherein the C6-C8 aryloxy group is optionally substituted with one or two independently selected C1-C6 alkyl groups. In an embodiment of Formulas 1, 2, and 3, R is an unsubstituted C1-C6 alkyl group. In an embodiment of Formulas 1, 2, and 3, R is a methyl group. In another embodiment of Formulas 1, 2, and 3, R is a propyl group. In another embodiment of Formulas 1, 2, and 3, R is an isopropyl group. In a further embodiment of Formulas 1, 2, and 3, R is a butyl group. In a further embodiment of Formulas 1, 2, and 3, R is a tert-butyl group. In an embodiment of Formulas 1, 2, and 3, R is a pentyl group.
In an embodiment of Formulas 1 and 2, R is a C1-C6 alkyl group optionally substituted with an amino group, wherein the amino group is optionally substituted with one C6-C8 aryl group wherein the C6-C8 aryl group is optionally and independently substituted with one or more C1-C6 alkyl groups. In an embodiment of Formulas 1 and 2, R is a methyl group substituted with an amino group, wherein the amino group is optionally substituted with one C6-C8 aryl group wherein the C6-C8 aryl group is optionally and independently substituted with one or more C1-C6 alkyl groups. In another embodiment of Formulas 1 and 2, R is a methyl group substituted with an amino group, wherein the amino group is substituted with one C6-C8 aryl group wherein the C6-C8 aryl group is optionally and independently substituted with one or more C1-C6 alkyl groups. In another embodiment of Formulas 1 and 2, R is a methyl group substituted with an amino group, wherein the amino group is substituted with one C6-C8 aryl group wherein the C6-C8 aryl group is substituted with one or more independently selected C1-C6 alkyl groups. In an embodiment of Formulas 1 and 2, R is a methyl group substituted with an amino group, which is substituted with a phenyl group, which is optionally substituted with one or more independently selected C1-C6 alkyl groups. In a further embodiment of Formulas 1 and 2, R is a methyl group, which is substituted with an amino group, which is substituted with a phenyl group, which is optionally substituted with one propyl group. In a further embodiment of Formulas 1 and 2, R is a methyl group, which is substituted with an amino group, which is substituted with a phenyl group, which is optionally substituted with one isopropyl group.
In an embodiment of Formulas 1 and 2, R is a C1-C6 alkyl group optionally substituted with a four to seven membered heterocycle. In an embodiment of Formulas 1 and 2, R is a C1-C6 alkyl group substituted with a four to seven membered heterocycle that comprises nitrogen. In another embodiment of Formulas 1 and 2, R is a methyl group substituted with a four to seven membered heterocycle. In another embodiment of Formulas 1 and 2, R is a methyl group substituted with a four to seven membered heterocycle that comprises nitrogen. In a further embodiment of Formulas 1 and 2, R is a methyl group substituted with an imidazolidine group.
In an embodiment of Formulas 1, 2, and 3, R is a C1-C6 alkoxy group. In another embodiment of Formulas 1, 2, and 3, R is methoxy.
In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryloxy group. In an embodiment of Formulas 1, 2, and 3, R is a phenoxy group.
In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one or more independently selected C1-C4 alkyl groups. In an embodiment of Formulas 1, 2, and 3, R is an unsubstituted C6-C8 aryl group. In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one or more methyl groups. In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one or more propyl groups. In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group substituted with two methyl groups. In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group substituted with two propyl groups. In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one or more isopropyl groups. In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group substituted with two isopropyl groups. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group optionally substituted with one or more methyl groups. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group optionally substituted with one or more propyl groups. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group optionally substituted with one or more isopropyl groups. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group substituted with two methyl groups. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group substituted with two propyl groups. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group substituted with two isopropyl groups.
In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one or more independently selected C1-C4 haloalkyl groups. In another embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one halomethyl group. In another embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one trifluoromethyl group. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group optionally substituted with one or more independently selected C1-C4 haloalkyl groups. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group optionally substituted with one halomethyl group. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group substituted with one trifluoromethyl group.
In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one or more independently selected C1-C4 haloalkoxy groups. In another embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one halomethoxy group. In another embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one trifluoromethoxy group. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group optionally substituted with one or more independently selected C1-C4 haloalkoxy groups. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group optionally substituted with one halomethoxy group. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group substituted with one trifluoromethoxy group.
In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one or more independently selected halogens. In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group optionally substituted with one halogen. In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group substituted with two halogens. In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group substituted with one or more fluorines. In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group substituted with one fluorine. In an embodiment of Formulas 1, 2, and 3, R is a C6-C8 aryl group substituted with two fluorines. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group substituted with one halogen. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group substituted with two halogens. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group substituted with one or more fluorines. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group substituted with one fluorine. In an embodiment of Formulas 1, 2, and 3, R is a phenyl group substituted with two fluorines.
In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group optionally substituted with one or more oxo groups. In an embodiment of Formulas 1, 2, and 3, R is a four membered heterocycle. In another embodiment of Formulas 1, 2, and 3, R is a four membered heterocycle optionally substituted with an oxo group. In an embodiment of Formulas 1, 2, and 3, R is a five membered heterocycle. In another embodiment of Formulas 1, 2, and 3, R is a five membered heterocycle optionally substituted with an oxo group. In another embodiment of Formulas 1, 2, and 3, R is a six membered heterocycle. In another embodiment of Formulas 1, 2, and 3, R is a six membered heterocycle optionally substituted with an oxo group.
In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group that comprises nitrogen. In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group that comprises two or more nitrogens. In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group that comprises at least one of both nitrogen and oxygen. In a further embodiment of Formulas 1, 2, and 3, R is a piperidine group. In another embodiment of Formulas 1, 2, and 3, R is a morpholine group. In an embodiment of Formulas 1, 2, and 3, R is a pyrrolidine group. In a further embodiment of Formulas 1, 2, and 3, R is an imidazolidine group. In another embodiment of Formulas 1, 2, and 3, R is an azetidine group optionally substituted with one or more oxo groups. In another embodiment of Formulas 1, 2, and 3, R is an unsubstituted azetidine group. In another embodiment of Formulas 1, 2, and 3, R is an azetidine group substituted with one oxo group.
In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group optionally substituted with one or more independently selected C1-C4 alkyl groups. In an embodiment of Formulas 1, 2, and 3, R is an unsubstituted four to seven membered heterocycle group. In an embodiment of Formulas 1, 2, and 3, R is an unsubstituted four to seven membered heterocycle group that comprises one or more nitrogens. In an embodiment of Formulas 1, 2, and 3, R is an unsubstituted four to seven membered heterocycle group that comprises one nitrogen. In an embodiment of Formulas 1, 2, and 3, R is an unsubstituted four to seven membered heterocycle group that comprises two nitrogens. In an embodiment of Formulas 1, 2, and 3, R is an unsubstituted four to seven, or five to seven, membered heterocycle group that comprises three nitrogens. In an embodiment of Formulas 1, 2, and 3, R is a pyrrolidine group. In an embodiment of Formulas 1, 2, and 3, R is a triazole group.
In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group substituted with one C1-C4 alkyl group. In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group substituted with one methyl group. In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group substituted with two C1-C4 alkyl groups. In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group substituted with two methyl groups. In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group that comprises one or more oxygen and is optionally substituted with one or more independently selected C1-C4 alkyl groups. In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group that comprises one or more nitrogen and is optionally substituted with one or more independently selected C1-C4 alkyl groups. In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group that comprises one or more oxygen and one or more nitrogen and is optionally substituted with one or more independently selected C1-C4 alkyl groups. In an embodiment of Formulas 1, 2, and 3, R is a morpholine group that is optionally substituted with one or more independently selected C1-C4 alkyl groups. In an embodiment of Formulas 1, 2, and 3, R is a piperazine group that is optionally substituted with one or more independently selected C1-C4 alkyl groups. In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group that comprises oxygen and nitrogen and is optionally substituted with two methyl groups. In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle group that comprises two nitrogens and is optionally substituted with one methyl group. In an embodiment of Formulas 1, 2, and 3, R is a morpholinyl group that is substituted with two methyl groups. In an embodiment of Formulas 1, 2, and 3, R is a piperazine group that is substituted with one methyl group. In an embodiment of Formulas 1, 2, and 3, R is a diazepane group that is substituted with one methyl group.
In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle optionally substituted with one or more oxo groups. In an embodiment of Formulas 1, 2, and 3, R is a four to seven membered heterocycle that comprises nitrogen and is optionally substituted with one or more oxo groups. In an embodiment of Formulas 1, 2, and 3, R is a pyrrolidine group optionally substituted with an oxo group. In an embodiment of Formulas 1, 2, and 3, R is a pyrrolidine group substituted with an oxo group.
In an embodiment of Formulas 1, 2, and 3, R is a nine to ten membered heterocycle having two ring structures. In an embodiment of Formulas 1, 2, and 3, R is a nine to ten membered heterocycle comprising at least one nitrogen and having two ring structures. In an embodiment of Formulas 1, 2, and 3, R is a nine to ten membered heterocycle comprising at least one oxygen and having two ring structures. In another embodiment of Formulas 1, 2, and 3, R is a nine to ten membered heterocycle comprising at least two oxygens and having two ring structures. In another embodiment of Formulas 1, 2, and 3, R is a nine to ten membered heterocycle comprising at least two oxygens and at least one nitrogen and having two ring structures. In an embodiment of Formulas 1, 2, and 3, R is a nine to ten membered heterocycle having two ring structures, one of which is a furan. In an embodiment of Formulas 1, 2, and 3, R is 2,3-dihydro-benzofuran. In an embodiment of Formulas 1, 2, and 3, R is a nine to ten membered heterocycle having two ring structures, one of which is a dioxolane. In an embodiment of Formulas 1, 2, and 3, R is a nine to ten membered heterocycle having two ring structures, one of which is a piperidine. In an embodiment of Formulas 1, 2, and 3, R is a nine to ten membered heterocycle having two ring structures, one of which is a pyrrolidine. In an embodiment of Formulas 1, 2, and 3, R is a nine to ten membered heterocycle having two ring structures, one of which is a dioxolane. In an embodiment of Formulas 1, 2, and 3, R is 1,4-dioxa-8-aza-spiro-[4.5]decane. In an embodiment of Formulas 1, 2, and 3, R is a nine to ten membered heterocycle having two ring structures, one of which is a pyrrolidine. In an embodiment of Formulas 1, 2, and 3, R is an indane.
In an embodiment of Formulas 1 and 2, R is an amino group optionally substituted with one or two independently selected C1-C6 alkyl groups, each of which is optionally and independently substituted with a hydroxy group, a C6-C8 aryl group, or a nine to ten membered heterocycle having two ring structures. In an embodiment of Formula 3, R is an amino group optionally substituted with one or two independently selected C1-C6 alkyl groups, each of which is optionally and independently substituted with a hydroxy group, a phenyl group, or a benzo[1,3]-dixoxole group. In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with an ethyl group, wherein the ethyl group is optionally substituted with a hydroxy group. In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with a butyl group, wherein the butyl group is optionally substituted with a hydroxy group. In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with a hexyl group, wherein the hexyl group is optionally substituted with a hydroxy group. In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with an ethyl group, wherein the ethyl group is substituted with a hydroxy group. In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with a butyl group, wherein the butyl group is substituted with a hydroxy group. In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with a hexyl group, wherein the hexyl group is substituted with a hydroxy group.
In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with an ethyl group, wherein the ethyl group is optionally substituted with a phenyl group. In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with a propyl group, wherein the propyl group is optionally substituted with a phenyl group. In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with an ethyl group, wherein the ethyl group is substituted with a phenyl group. In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with a propyl group, wherein the propyl group is substituted with a phenyl group. In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with a pentyl group, wherein the pentyl group is optionally substituted with a hydroxy group. In an embodiment of Formulas 1, 2, and 3, R is an amino group substituted with a pentyl group, wherein the pentyl group is substituted with a hydroxy group.
In an embodiment of Formulas 1, 2, and 3, R is an amino group optionally substituted with two methyl groups, both of which are optionally and independently substituted with a phenyl group. In an embodiment of Formulas 1, 2, and 3, R is an amino group optionally substituted with two methyl groups, one of which is substituted with a phenyl group.
In an embodiment of Formulas 1, 2, and 3, R is an amino group optionally substituted with one or two independently selected C6-C8 aryl groups. In an embodiment of Formulas 1, 2, and 3, R is an amino group optionally substituted with a phenyl group.
In an embodiment of Formulas 1, 2, and 3, R is a carboxy group.
In an embodiment of Formulas 1, 2, and 3, R is a carbonyl group substituted with a five to six membered heterocycle group. In an embodiment of Formulas 1, 2, and 3, R is a carbonyl group substituted with a five membered heterocycle group. In another embodiment of Formulas 1, 2, and 3, R is a carbonyl group substituted with a six membered heterocycle group. In an embodiment of Formulas 1, 2, and 3, R is a carbonyl group substituted with a five to six membered heterocycle group that comprises nitrogen. In an embodiment of Formulas 1, 2, and 3, R is a carbonyl group substituted with a pyrrolidine group.
In an embodiment of Formulas 1, 2, and 3, each R is an independently selected halogen. In an embodiment of Formulas 1, 2, and 3, R is chlorine. In another embodiment of Formulas 1, 2, and 3, R is bromine. In a further embodiment of Formulas 1, 2, and 3, R is fluorine.
In another embodiment of Formulas 1, 2, and 3, R is a carbonyl group substituted with a five to six membered heterocycle group. In a further embodiment of Formulas 1, 2, and 3, R is a carbonyl group substituted with a heterocycle that comprises oxygen. In a further embodiment of Formulas 1, 2, and 3, R is a carbonyl group substituted with a heterocycle that comprises nitrogen. In a further embodiment of Formulas 1, 2, and 3, R is a carbonyl group substituted with a heterocycle that comprises oxygen and nitrogen. In another embodiment of Formulas 1, 2, and 3, R is a carbonyl group substituted with a morpholine group.
In another embodiment of Formulas 1, 2, and 3, two R groups together with the hetero-bicycle to which they are attached form a twelve to thirteen membered heterocycle having three ring structures. In an embodiment of Formulas 1, 2, and 3, two alkoxy groups together with the hetero-bicycle to which they are attached form a twelve to thirteen membered ring. In an embodiment of Formulas 1, 2, and 3, two methoxy groups together with the hetero-bicycle to which they are attached form a twelve to thirteen membered ring. In an embodiment of Formulas 1 and 2, one alkoxy and one oxy group together with the hetero-bicycle to which they are attached form a twelve to thirteen membered ring. In an embodiment of Formulas 1 and 2, a methoxy and an oxy group together with the hetero-bicycle to which they are attached form a twelve to thirteen membered ring.
In another embodiment of Formulas 1, 2, and 3, W is N, Y is C, and Z is N. In a further embodiment of Formulas 1, 2, and 3, W is N, Y is C, Z is N, and n is 0. In a further embodiment of Formulas 1, 2, and 3, W is N, Y is C, Z is N, n is 0, and R2 is C6 to C8 aryl. In another embodiment of Formulas 1, 2, and 3, W is N, Y is C, Z is N, n is 0, and R2 is a phenyl group.
In a further embodiment of Formulas 1, 2, and 3, W is N, Y is C, Z is N, and n is 1. In another embodiment of Formulas 1, 2, and 3, W is N, Y is C, Z is N, n is 1, and R is a halogen. In another embodiment of Formulas 1, 2, and 3, W is N, Y is C, Z is N, n is 1, R is a halogen, and R2 is C6 to C8 aryl. In a further embodiment of Formulas 1, 2, and 3, W is N, Y is C, Z is N, n is 1, R is a halogen, and R2 is a phenyl group.
As recognized by one of skill in the art, certain compounds of the invention may include at least one chiral center, and as such may exist as racemic mixtures or as enantiomerically pure compositions. As used herein, “enantiomerically pure” refers to compositions consisting substantially of a single isomer, preferably consisting of 90%, 92%, 95%, 98%, 99%, or 100% of a single isomer.
As used herein, the term “alkyl” generally refers to saturated hydrocarbyl radicals of straight, branched or cyclic configuration including methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, n-hexyl, cyclohexyl, n-heptyl, octyl, n-octyl, and the like. In some embodiments, alkyl substituents may be C1 to C8, C1 to C6, or C1 to C4 alkyl groups. In certain embodiments, the alkyl group may be optionally substituted with one or more independently selected halogen or alkoxy groups. For instance, the alkyl group may be a haloalkyl, including monohaloalkyl, dihaloalkyl, and trihaloalkyl.
As used herein, “alkenyl” generally refers to linear, branched or cyclic alkene radicals having one or more carbon-carbon double bonds, such as C2 to C6 alkylene groups including 3-propenyl.
As used herein, “aryl” refers to a carbocyclic aromatic ring structure. Included in the scope of aryl groups are aromatic rings having from five to twenty carbon atoms. Aryl ring structures include compounds having one or more ring structures, such as mono-, bi-, or tricyclic compounds. Examples of aryl groups that include phenyl, tolyl, anthracenyl, fluorenyl, indenyl, azulenyl, phenanthrenyl (i.e., phenanthrene), and napthyl (i.e., napthalene) ring structures. In certain embodiments, the aryl group may be optionally substituted.
As used herein, “heterocycle” refers to cyclic ring structures in which one or more atoms in the ring, the heteroatom(s), is an element other than carbon. Heteroatoms are typically O, S or N atoms. Included within the scope of heterocycle, and independently selectable, are O, N, and S heterocycle ring structures. The ring structure may include compounds having one or more ring structures, such as mono-, bi-, or tricyclic compounds, and may be aromatic, i.e., the ring structure may be a heteroaryl. Example of heterocyclo groups include morpholinyl, pyrrolidinonyl, pyrrolidinyl, piperidinyl, piperazinyl, hydantoinyl, valerolactamyl, oxiranyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, tetrahydropyridinyl, tetrahydroprimidinyl, tetrahydrothiophenyl or tetrahydrothiopyranyl and the like. In certain embodiments, the heterocycle may optionally be substituted.
As used herein, “heteroaryl” refers to cyclic aromatic ring structures in which one or more atoms in the ring, the heteroatom(s), is an element other than carbon. Heteroatoms are typically O, S or N atoms. Included within the scope of heteroaryl, and independently selectable, are O, N, and S heteroaryl ring structures. The ring structure may include compounds having one or more ring structures, such as mono-, bi-, or tricyclic compounds. In some embodiments, the heteroaryl groups may be selected from heteroaryl groups that contain two or more heteroatoms, three or more heteroatoms, or four or more heteroatoms. Heteroaryl ring structures may be selected from those that contain five or more atoms, six or more atoms, or eight or more atoms. In a preferred embodiment, the heteroaryl including five to ten atoms. Examples of heteroaryl ring structures include: acridine, benzimidazole, benzoxazole, benzodioxole, benzofuran, 1,3-diazine, 1,2-diazine, 1,2-diazole, 1,4-diazanaphthalene, furan, furazan, imidazole, indole, isoxazole, isoquinoline, isothiazole, oxazole, purine, pyridazine, pyrazole, pyridine, pyrazine, pyrimidine, pyrrole, quinoline, quinoxaline, thiazole, thiophene, 1,3,5-triazine, 1,2,4-triazine, 1,2,3-triazine, tetrazole and quinazoline.
As used herein, “alkoxy” generally refers to a group with the structure —O—R. In certain embodiments, R may be an alkyl group, such as a C1 to C8, C1 to C6 alkyl group, or C1 to C4 alkyl group. In certain embodiments, the R group of the alkoxy may optionally be substituted with at least one halogen. For example, the R group of the alkoxy may be a haloalkyl, i.e., haloalkoxy.
Halogen substituents may be independently selected from the halogens such as fluorine, chlorine, bromine, iodine, and astatine.
For the purposes of this invention, where one or more functionalities or substituents are incorporated into a compound of the invention, including preferred embodiments, each functionality or substituent appearing at any location within the disclosed compounds may be independently selected, and as appropriate, independently substituted. Further, where a more generic substituent is set forth for any position in the molecules of the present invention, it is understood that the generic substituent may be replaced with more specific substituents, and the resulting molecules are within the scope of the molecules of the present invention.
With reference to Formulas 1 and 2, Ra is preferably independently selected from: a halogen; a C1 to C6 alkyl; a C1 to C6 haloalkyl; a C1 to C6 alkoxy; a C1 to C6 haloalkoxy; a C6 to C8 aryl group; a carboxy group; a carbamoyl group; an amino group which is optionally substituted.
In one embodiment, the four to seven membered heterocycles of Formulas 1, 2, and 3 are preferably selected from: an azetidine group, a pyrrolidine group, a piperidine group, a piperazine group, a morpholine group, a [1,4]diazepane group, a pyrazole group, an imidazole group, a [1,2,4] triazole group, a pyridine group, a furan group, and a thiophene group. Further, the four to seven membered heterocycles may be optionally substituted as illustrated in Formulas 1, 2, and 3.
In another embodiment of Formulas 1, 2, and 3, the nine to ten membered heterocycle having two ring structures is preferably selected from the group consisting of a benzofuran group, a 2,3-dihydro-benzofuran group, a benzo[1,3]dioxole group, a 2,3-dihydro-isoindole group, a 2,3-dihydro-indole group, a 1,2,3,4-tetrahydro-isoquinoline group, and a 1,4-dioxa-8-aza-spiro[4.5]decane group.
In yet another preferred embodiment of Formulas 1, 2, and 3, R2 is preferably selected from the following, wherein the * indicates the bond of attachment:
In yet another preferred embodiment of Formulas 1, 2, and 3, R is preferably selected from the following, wherein the * indicates the bond of attachment:
In a preferred embodiment of Formulas 1, 2, and 3, Y is C, Z is N, and R1 is absent (Formula 1/2/3-A):
With reference to Formula 1/2/3-A, n is preferably 1 or 2, and R group is in the 5 and/or 6 position. In an embodiment of Formula 1/2/3-A, R is preferably a carboxy group. Further, in an embodiment of Formula 1/2/3-A R2 is a C6 to C8 aryl, optionally substituted with one, two, or three —Ra groups, wherein Ra is preferably independently selected from: a halogen; a C1 to C6 alkyl; a C1 to C6 haloalkyl; a C1 to C6 alkoxy; a C1 to C6 haloalkoxy; a carboxy group; a carbamoyl group; an amino group which is optionally substituted; or a four to six membered heterocycle optionally substituted with an oxo group. In a preferred embodiment of Formula 1/2/3-A R2 is a C6 to C8 aryl, optionally substituted with one, two, or three —Ra groups, wherein Ra is preferably independently selected from: a halogen; a C1 to C6 alkyl; a C1 to C6 alkoxy; a C1 to C6 haloalkoxy; a carboxy group; a carbamoyl group; an amino group which is optionally substituted; or a four to six membered heterocycle optionally substituted with an oxo group. In a particularly preferred embodiment of Formula 1/2/3-A, R2 is a phenyl group optionally substituted with a carboxy group.
In a preferred embodiment of Formula of Formula 1/2/3-A, W is CH, n is 1, and R is a carboxy group and is located in the 5-position, as follows (Formula 1/2/3-A-1):
In another preferred embodiment of Formula 1/2/3-A, W is CH, n is 1, and R is a carboxy group and is located in the 6-position, as follows (Formula 1/2/3-A-2):
In yet another preferred embodiment of Formula 1/2/3-A, R2 is a phenyl group substituted with a carboxy group, W is CH, n is 1, and R is located in the 5-position, as follows (Formula 1/2/3-A-3):
In accordance with Formula 1/2/3-A-3, the carboxy group is preferably in a meta or para position. Further, in accordance with an embodiment of Formula 1/2/3-A-3, R is a halogen; a carboxy group; a C1-C6 alkyl group; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a phenyl, or a benzo[1,3]dioxole group; a carbonyl group substituted with a five to six membered heterocycle group; or a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; or a nine to ten membered heterocycle having two ring structures. In an embodiment of Formula 1/2/3-A-3, R is a halogen; a carboxy group; a C1-C6 alkyl group; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a phenyl, or a benzo[1,3]dioxole group; a carbonyl group substituted with a five to six membered heterocycle group; or a four to seven membered heterocycle group optionally substituted with one more oxo groups; or a nine to ten membered heterocycle having two ring structures. In another preferred embodiment of Formula 1/2/3-A-3, R is selected from a halogen, a C1 to C6 alkyl, or a C6 to C8 aryl.
In yet another preferred embodiment of Formula 1/2/3-A, R2 is a phenyl group substituted with a carboxy group, W is CH, n is 1, and R is located in the 6-position, as follows (Formula 1/2/3-A-4):
In an embodiment of Formula 1/2/3-A-4, the carboxy group is preferably in a meta or para positions. Further, R is a halogen; a carboxy group; a C1-C6 alkyl group optionally substituted with a C6-C8 aryloxy group, an imidazole group, or an amino group which is optionally substituted with one or two independently selected C1-C6 alkyl or C6-C8 aryl groups; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; a carbonyl group substituted with a five to six membered heterocycle group; a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; or a nine to ten membered heterocycle having two ring structures. In a preferred embodiment of Formula 1/2/3-A-4, R is a halogen; a carboxy group; a C1-C6 alkyl group; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C1-C6 alkyl groups, which are optionally and independently substituted with a hydroxy, a phenyl, or a benzo[1,3]dioxole group; a carbonyl group substituted with a five to six membered heterocycle group; or a four to seven membered heterocycle group optionally substituted with one more oxo groups; or a nine to ten membered heterocycle having two ring structures. In another preferred embodiment of Formula 1/2/3-A-4, R is selected from is a halogen or a carboxy group.
In yet another preferred embodiment of Formula 1, 2, and 3-A, R2 is a phenyl group substituted with a carbamoyl group, W is CH, n is 1, and R is located in the 5-position, as follows (Formula 1/2/3-A-5):
In an embodiment of Formula 1/2/3-A-5, the carbamoyl group is preferably in a meta or para positions. Further, in an embodiment of Formula 1/2/3-A-5, R is a halogen; a carboxy group; a C1-C6 alkyl group; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a phenyl, or a benzo[1,3]dioxole group; a carbonyl group substituted with a five to six membered heterocycle group; or a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; or a nine to ten membered heterocycle having two ring structures. In a preferred embodiment of Formula 1/2/3-A-5, R is a halogen; a C1-C6 alkyl group; a C1-C6 alkoxy; a C6-C8 aryloxy; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a phenyl; or a four to seven membered heterocycle group.
In yet another preferred embodiment of Formula 1/2/3-A, R2 is a phenyl group substituted with a carbamoyl group, W is CH, n is 1, and R is located in the 6-position, as follows (Formula 1/2/3-A-6):
In an embodiment of Formula 1/2/3-A-6, the carbamoyl group is preferably in a meta or para positions. Further, R is selected from the group consisting of a halogen; a carboxy group; a C1-C6 alkyl group optionally substituted with a C6-C8 aryloxy group, an imidazole group, or an amino group which is optionally substituted with one or two independently selected C1-C6 alkyl or C6-C8 aryl groups; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; a carbonyl group substituted with a five to six membered heterocycle group; a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; and a nine to ten membered heterocycle having two ring structures. In a preferred embodiment of Formula 1/2/3-A-6, R is a halogen; a C1-C6 alkyl group; a C1-C6 alkoxy; a C6-C8 aryloxy; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a phenyl; or a four to seven membered heterocycle group.
In another preferred embodiment, Y is N, Z is C, W is CH, and R2 is absent (Formula 1/2/3-B):
With reference to Formula 1/2/3-B, in an embodiment, R1 is preferably a phenyl group optionally substituted with a carboxy group. Further, in another embodiment of Formula 1/2/3-B, R is a C1-C6 alkyl; a C1-C6 alkoxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; or two R groups together with the hetero-bicycle to which they are attached form a twelve to thirteen membered heterocycle having three ring structures.
In a preferred embodiment of Formula 1/2/3-B, the twelve to thirteen membered heterocycle is selected from the following, wherein the * indicates the bond of attachment to R1:
In another embodiment, preferred compounds of the invention also include the compounds of Formula 4:
wherein:
Y and Z are independently selected from N or C;
W is N or CH;
R1 is hydrogen, a C6 to C8 aryl which is optionally substituted with a carboxy group, or R1 is absent when Z is N;
R2 is hydrogen; a C6 to C8 aryl which is optionally substituted with one, two, or three independently selected Ra groups; a four to seven membered heterocycle which is optionally substituted with one or more independently selected C1-C6 alkyl groups or a three to seven membered heterocycle; or R2 is absent when Y is N;
R3 is absent; a halogen; a carboxy group; an alkoxy group; or R3, wherein R3 may also include an oxy group, together with R4 and the heterocycle to which they are attached preferably form a twelve to thirteen membered heterocycle with three ring structures;
R4 is absent, a halogen; a carboxy group; a C1-C6 alkyl group; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; an amino group optionally substituted with one or two independently selected C6-C8 aryl or C1-C6 alkyl groups, which are optionally substituted with a hydroxy, a phenyl, or a benzo[1,3]dioxole group; a carbonyl group substituted with a five to six membered heterocycle group; or a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; a nine to ten membered heterocycle having two ring structures; or R3 together with R4 and the heterocycle to which they are attached preferably form a twelve to thirteen membered heterocycle with three ring structures;
R5 is independently selected from: absent, a halogen; a carboxy group; a C1-C6 alkyl group optionally substituted with a C6-C8 aryloxy group, an imidazole group, or an amino group which is optionally substituted with one or two independently selected C1-C6 alkyl or C6-C8 aryl groups; a C1-C6 alkoxy; a C6-C8 aryloxy; a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups; a carbonyl group substituted with a five to six membered heterocycle group; a four to seven membered heterocycle group optionally substituted with one more C1-C4 alkyl or oxo groups; or a nine to ten membered heterocycle having two ring structures;
or a pharmaceutically acceptable salt, hydrate, solvate, clathrate, racemate, stereoisomer, or polymorph of said compound of Formula 4.
In a preferred embodiment of Formula 4, R3 is hydrogen, halogen, or a carboxy group. In another embodiment, wherein R3 may optionally be an oxy group, R3 together with R4 and the heterocycle to which they are attached preferably form a twelve to thirteen membered heterocycle with three ring structures.
In a preferred embodiment of Formula 4, R4 is selected from:
In yet another preferred embodiment of Formula 4, R5 is selected from the following, wherein the * indicates the bond of attachment:
In a preferred embodiment of Formula 4, Y is C, Z is N, and R1 is absent (Formula 4-A):
With reference to Formula 4-A, R2 is preferably a C6 to C8 aryl, optionally substituted with one, two, or three —Ra groups, wherein Ra is independently selected from: a halogen; a C1 to C6 alkyl; a C1 to C6 haloalkyl; a C1 to C6 alkoxy; a C1 to C6 haloalkoxy; a C6 to C8 aryl group; a carboxy group; a carbamoyl group; an amino group which is optionally substituted with one or two independently selected hydroxy groups, halogens, C1 to C6 alkyls, or C1 to C6 haloalkyls; or a four to six membered heterocycle optionally substituted with an oxo group. In a particularly preferred embodiment, R2 is a phenyl group optionally substituted with a carboxy group.
In another preferred embodiment of Formula 4, Y is N, Z is C, W is CH and R2 is absent (Formula 4-B):
With reference to Formula 4-B, R1 is a phenyl group optionally substituted with a carboxy group. Further, R3 is preferably hydrogen, a halogen, or a carboxy group. R4 and R5 are preferably independently selected from: hydrogen, a C1-C6 alkyl group, a C1-C6 alkoxy group, or a C6-C8 aryl optionally substituted with one or more independently selected halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, or C1-C4 haloalkoxy groups. In another embodiment, R3 together with R4 and the heterocycle to which they are attached preferably form a twelve to thirteen membered heterocycle with three ring structures. In a preferred embodiment, the twelve to thirteen membered heterocycle is selected from the following, wherein the * indicates the bond of attachment to R1:
Preferred compounds of the invention include the following.
Particularly preferred compounds are Compound NOs: 19, 20, 42, 49, 53, 56, 58, 59, 85, 91, 94, 96, 100, 101, 102.
The above compounds are listed only to provide examples that may be used in the methods of the invention. Based upon the instant disclosure, the skilled artisan would recognize other compounds intended to be included within the scope of the presently claimed invention that would be useful in the methods recited herein.
B. Preparation of Compounds of the Invention
Compounds of the invention may be produced in any manner known in the art. By way of example, certain benzooxazole compounds of Formulas 1-A and 2-A may be prepared in the manner shown in Scheme A.
In accordance with Scheme A, m (or p)-cyanato methyl benzoate (I) may be synthesized as follows. A solution of m (or p)-cyanobenzoic acid (1.0 equiv.) and K2CO3 (1.5 equiv.) in DMF is treated with iodomethane (1.5 equiv.) and stirred at room temperature for 5 h until the complete consumption of the starting material. The reaction mixture is poured into ice-water to afford a white crystalline solid which is collected by filtration and washed with water and hexanes in sequence.
Compound (I) is then used in the synthesis of m (or p)-methoxycarboniumidoyl-benzoic acid methyl ester hydrochloride (II) as follows. Compound (I) (1.0 equiv.) is dissolved in methanol, acetyl chloride (>20.0 equiv.) is added to the solution at room temperature under stirring. After 5˜6 h, the mixture is dried under reduced pressure to give a crude product which was washed with ethyl ether to obtain a pure product.
Compound (II) is then used in the synthesis of m (or p) benzooxazol-2-yl-benzoic acid methyl ester and its analogues (III) as follows. A mixture of compound (II) (1.0 equiv.) and aminophenol (or substituted aminophenols) in methanol is refluxed for 2-8 h. Methanol is evaporated. The residue is purified by flash chromatography (gradient elution using ethyl acetate-hexanes or methanol-methylene chloride in different ratio) to afford the desired compound (III).
Finally, compound (III) is used in the synthesis of m (or p) benzooxazol-2-yl-benzoic acid (IV) as follows. Compound (III) (1.0 equiv.) and LiI (>10.0 equiv.) is suspended in dry pyridine. The mixture is refluxed for 5 h˜overnight until invisible starting material by TLC. 1N HCl is added to the reaction mixture until PH<7. The resulting acidic mixture is extracted with ethyl acetate (2˜3 times). The combined ethyl estate is dried over Mg2SO4, and evaporated under reduced pressure to give the crude product followed by washing with ethyl ether or recrystallization for further purification to obtain the product, compound (IV)
In another embodiment, benzooxazole compounds of Formula 1-A and 2-A may be synthesized using a palladium catalyzed Suzuki coupling reaction, as shown in Scheme B. See, e.g., Nicholas E. Leadbeater and Maria Marco. Organic Letters. 2002, 4(17), 2973-2976.
In accordance with Scheme B, compounds of the invention may generally be synthesized as follows. In a 10 ml glass tube are placed 3-(5-bromo-benzooxazole-2-yl)benzoic acid methyl ester (1.0 equiv.), substituted phenylboronic acid (1.0 equiv.), Na2CO3 (3.0 equiv.), t-butylammonia iodide (TBAI, as a phase-transfer catalyst, 1.0 equiv.), 6-8 ml of H2O, and a stirring bar. The vessel is sealed and placed into the microwave cavity. 60 w of power and 150° C. is used for the reaction condition. The reaction is held for 5-10 min. and detected by LC-MS for the complete conversion of the starting materials to the desired product. The reaction mixture is acidified using 1N HCl until PH<7, and partitioned between ethyl acetate and water. Water layer is extracted with ethyl acetate 3 times. Ethyl acetate is combined and washed with Brine (in most of the cases, solid is crushed out in organic phase), then dried over Mg2SO4 and evaporated. The residue is washed with ethyl ether to afford the desired product as a crystalline solid (in some cases, recrystallization is needed to improve the purity).
In yet another embodiment, benzooxazole compounds of Formula 1-A and 2-A may be synthesized using a copper catalyzed amidation reaction, as shown in Scheme C. See, e.g., Artis Klapars, Xiaohua Huang, and Stephen L. Buchwald. J. Am. Chem. Soc. 2002, 124, 7421-7428.
In accordance with Scheme C, compounds of the invention may generally be synthesized as follows. A 50 ml culture tube is placed with 3-(5-bromo-benzooxazole-2-yl)benzoic acid methyl ester (1.0 equiv.), CuI (5.0% equiv.), Cyclic amide (1.25 equiv.), and K2CO3 (2.0 equiv.), evacuated, and backed charged with N2. Trans-diamino-cyclohexane (10.0% equiv.) and toluene (2.0-3.0 ml) are added under N2. The tube is sealed with a Teflon cap and the reaction mixture is stirred at 110° C. for 15-20 h, or until no further reaction proceeding. The resulting reaction mixture is added water, and extracted with ethyl acetate. The organic layer is washed with H2O to afford a colorful solid which is purified by flash chromatography using a mixture of ethyl acetate-hexanes followed by methanol-methylene chloride in different ratio to provide desired product as a solid.
In yet another embodiment, benzooxazole compounds of Formula 1-A and 2-A may be synthesized using a commercial unavailable amino phenols and aromatic nucleophilic substitution section, as shown in Scheme D.
In accordance with Scheme D, compounds of the invention may generally be synthesized as follows. A mixture of 5-fluoro-2-nitrophenol (1.0 equiv.), amines (1.5-3.0 equiv.) in DMSO (4.0-10.0 ml) is charged in a 50 ml culture tube and stirred at room temperature to 98° C. for 2 h-overnight. Yellow solid is precipitated by addition of water. Desired product is collected by filtration and washed with water, hexanes in sequence. The obtained product from the above reaction is dissolved or suspended in methanol (20-30 ml), and is added with 20% (by weight) of Pd/C. The mixture is shacked at room temperature using ˜55 psi hydrogen for 5-8 h until complete consumption of the starting material by TLC. Methanol is removed, and the residue is used for the next step without purification (see, e.g., final step of Scheme C above)
Schemes E, F, G, and H may generally be used to synthesize the compounds of Formula 1-B and 2-B, as follows.
In certain preferred embodiments, compounds of the invention may be resolved to enantiomerically pure compositions or synthesized as enantiomerically pure compositions using any method known in art. By way of example, compounds of the invention may be resolved by direct crystallization of enantiomer mixtures, by diastereomer salt formation of enantiomers, by the formation and separation of diasteriomers or by enzymatic resolution of a racemic mixture.
These and other reaction methodologies may be useful in preparing the compounds of the invention, as recognized by one of skill in the art. Various modifications to the above schemes and procedures will be apparent to one of skill in the art, and the invention is not limited specifically by the method of preparing the compounds of the invention.
C. Methods of the Invention
In another aspect of the invention, methods are provided for the suppression of premature translation termination, which may be associated with a nonsense mutation, and for the prevention or treatment of diseases. In a preferred embodiment, such diseases are associated with mutations of mRNA, especially nonsense mutations. Exemplary diseases include, but are not limited to, cancer, lysosomal storage disorders, the muscular dystrophies, cystic fibrosis, hemophilia, epidermolysis bullosa and classical late infantile neuronal ceroid lipofuscinosis. In this embodiment, methods for treating cancer, lysosomal storage disorders, a muscular dystrophy, cystic fibrosis, hemophilia, or classical late infantile neuronal ceroid lipofuscinosis are provided comprising administering a therapeutically effective amount of at least one compound of the invention to a subject in need thereof.
In one embodiment, the present invention is directed to methods for increasing the expression of one or more specific, functional proteins. Any compound of the invention can be used to specifically increase expression of functional protein. In another embodiment, a specific increase in expression of functional protein occurs when premature translation termination is suppressed by administering a therapeutically effective amount of at least one compound of the invention to a subject in need thereof. In a preferred embodiment premature translation termination is associated with a nonsense mutation in mRNA. In another embodiment, a specific increase in expression of functional protein occurs when mRNA decay is reduced in a patient. In a preferred embodiment, the abnormality in a patient is caused by mutation-mediated mRNA decay. In a particularly preferred embodiment, mutation-mediated mRNA decay is the result of a nonsense mutation. The methods of the present invention are not limited by any particular theory.
The invention encompasses methods of treating and preventing diseases or disorders ameliorated by the suppression of premature translation termination, nonsense-mediated mRNA decay, or premature translation termination and nonsense-mediated mRNA decay in a patient which comprise administering to a patient in need of such treatment or prevention a therapeutically effective amount of a compound of the invention.
In one embodiment, the present invention encompasses the treatment or prevention of any disease that is associated with a gene exhibiting premature translation termination, nonsense-mediated mRNA decay, or premature translation termination and nonsense-mediated mRNA decay. In one embodiment, the disease is due, in part, to the lack of or reduced expression of the gene resulting from a premature stop codon. Specific examples of genes which may exhibit premature translation termination and/or nonsense-mediated mRNA decay and diseases associated with premature translation termination and/or nonsense-mediated mRNA decay are found in U.S. Provisional Patent Application No. 60/390,747, titled: Methods For Identifying Small Molecules That Modulate Premature Translation Termination And Nonsense Mediated mRNA Decay, filed Jun. 21, 2002, and International Application PCT/US03/19760, filed Jun. 23, 2003, both of which are incorporated herein by reference in their entirety.
Diseases ameliorated by the suppression of premature translation termination, nonsense-mediated mRNA decay, or premature translation termination and nonsense-mediated mRNA decay include, but are not limited to: genetic diseases, somatic diseases, cancers, autoimmune diseases, blood diseases, collagen diseases, diabetes, neurodegenerative diseases, proliferative diseases, cardiovascular diseases, pulmonary diseases, inflammatory diseases or central nervous system diseases.
In one embodiment, diseases to be treated or prevented by administering to a patient in need thereof an effective amount of a compound of the invention include, but are not limited to, amyloidosis, hemophilia, Alzheimer's disease, Tay Sachs disease, Niemann Pick disease, atherosclerosis, giantism, dwarfism, hypothyroidism, hyperthyroidism, aging, obesity, Parkinson's disease, cystic fibrosis, muscular dystrophy, heart disease, kidney stones, ataxia-telangiectasia, familial hypercholesterolemia, retinitis pigmentosa, Duchenne muscular dystrophy, epidermolysis bullosa and Marfan syndrome. In one embodiment, the diseases are associated with a nonsense mutation.
In one embodiment, the compounds of the invention are useful for treating or preventing an autoimmune disease. In one embodiment, the autoimmune disease is associated with a nonsense mutation. In a preferred embodiment, the autoimmune disease is rheumatoid arthritis or graft versus host disease.
In another embodiment, the compounds of the invention are useful for treating or preventing a blood disease. In one embodiment, the blood disease is associated with a nonsense mutation. In a preferred embodiment, the blood disease is hemophilia, Von Willebrand disease, ataxia-telangiectasia, β-thalassemia or kidney stones.
In another embodiment, the compounds of the invention are useful for treating or preventing a collagen disease. In one embodiment, the collagen disease is associated with a nonsense mutation. In a preferred embodiment, the collagen disease is osteogenesis imperfecta or cirrhosis.
In another embodiment, the compounds of the invention are useful for treating or preventing diabetes. In one embodiment, the diabetes is associated with a nonsense mutation.
In another embodiment, the compounds of the invention are useful for treating or preventing an inflammatory disease. In one embodiment, the inflammatory disease is associated with a nonsense mutation. In a preferred embodiment, the inflammatory disease is arthritis, rheumatoid arthritis or osteoarthritis.
In another embodiment, the compounds of the invention are useful for treating or preventing a central nervous system disease. In one embodiment, the central nervous system disease is associated with a nonsense mutation. In one embodiment, the central nervous system disease is a neurodegenerative disease. In a preferred embodiment, the central nervous system disease is multiple sclerosis, muscular dystrophy, Duchenne muscular dystrophy, Alzheimer's disease, Tay Sachs disease, Niemann Pick disease, late infantile neuronal ceroid lipofuscinosis (LINCL) or Parkinson's disease.
In another preferred embodiment, the compounds of the invention are useful for treating or preventing cancer, particularly in humans. In a preferred embodiment, the cancer is of the head and neck, eye, skin, mouth, throat, esophagus, chest, bone, blood, lung, colon, sigmoid, rectum, stomach, prostate, breast, ovaries, kidney, liver, pancreas, brain, intestine, heart or adrenals. In one embodiment, the cancer is a solid tumor. In one embodiment, the cancer is associated with a nonsense mutation. In another embodiment, the cancer is associated with a genetic nonsense mutation. In another embodiment, the cancer is associated with a somatic mutation. Without being limited by any theory, the use of the compounds of the invention against cancer may relate to its action against mutations of the p53 gene.
In one embodiment, the cancer is not a blood cancer. In another embodiment, the cancer is not leukemia. In another embodiment, the cancer is not multiple myeloma. In another embodiment, the cancer is not prostate cancer.
In another preferred embodiment, the compounds of the invention are useful for treating or preventing cancer associated with a mutation of tumor suppressor gene. Such genes include, but are not limited to PTEN, BRCA1, BRCA2, Rb, and the p53 gene. In one embodiment, the mutation is a genetic mutation. In another embodiment, the mutation is a somatic mutation. The methods of the invention are particularly useful for treating or preventing a cancer associated with a nonsense mutation in the in a tumor suppressor gene. In a preferred embodiment, the methods of the invention are particularly useful for treating or preventing a cancer associated with a p53 gene due to the role of p53 in apoptosis. Without being limited by theory, it is thought that apoptosis can be induced by contacting a cell with an effective amount of a compound of the invention resulting in suppression of the nonsense mutation, which, in turn, allows the production of full-length p53 to occur. Nonsense mutations have been identified in the p53 gene and have been implicated in cancer. Several nonsense mutations in the p53 gene have been identified (see, e.g., Masuda et al., 2000, Tokai J Exp Clin Med. 25(2):69-77; Oh et al., 2000, Mol Cells 10(3):275-80; Li et al., 2000, Lab Invest. 80(4):493-9; Yang et al., 1999, Zhonghua Zhong Liu Za Zhi 21(2):114-8; Finkelstein et al., 1998, Mol. Diagn. 3(1):37-41; Kajiyama et al., 1998, Dis Esophagus. 11(4):279-83; Kawamura et al., 1999, Leuk Res. 23(2):115-26; Radig et al., 1998, Hum Pathol. 29(11):1310-6; Schuyer et al., 1998, Int J Cancer 76(3):299-303; Wang-Gohrke et al., 1998, Oncol Rep. 5(1):65-8; Fulop et al., 1998, J Reprod Med. 43(2):119-27; Ninomiya et al., 1997, J Dermatol Sci. 14(3):173-8; Hsieh et al., 1996, Cancer Lett. 100(1-2):107-13; Rall et al., 1996, Pancreas. 12(1):10-7; Fukutomi et al., 1995, Nippon Rinsho. 53(11):2764-8; Frebourg et al., 1995, Am J Hum Genet. 56(3):608-15; Dove et al., 1995, Cancer Surv. 25:335-55; Adamson et al., 1995, Br J Haematol. 89(1):61-6; Grayson et al., 1994, Am J Pediatr Hematol Oncol. 16(4):341-7; Lepelley et al., 1994, Leukemia. 8(8):1342-9; McIntyre et al., 1994, J Clin Oncol. 12(5):925-30; Horio et al., 1994, Oncogene. 9(4):1231-5; Nakamura et al., 1992, Jpn J Cancer Res. 83(12):1293-8; Davidoff et al., 1992, Oncogene. 7(1):127-33; and Ishioka et al., 1991, Biochem Biophys Res Commun. 177(3):901-6; the disclosures of which are hereby incorporated by reference herein in their entireties). Any disease associated with a p53 gene encoding a premature translation codon including, but not limited to, the nonsense mutations described in the references cited above, can be treated or prevented by compounds of the invention.
In other embodiments, diseases to be treated or prevented by administering to a patient in need thereof an effective amount of a compound of the invention include, but are not limited to, solid tumors such as sarcoma, carcinomas, fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, pancreatic cancer, breast cancer, ovarian cancer, prostate cancer, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilms' tumor, cervical cancer, testicular tumor, lung carcinoma, small cell lung carcinoma, bladder carcinoma, epithelial carcinoma, glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, Kaposi's sarcoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, menangioma, melanoma, neuroblastoma, retinoblastoma, a blood-born tumor or multiple myeloma.
In another embodiment, diseases to be treated or prevented by administering to a patient in need thereof an effective amount of a compound of the invention include, but are not limited to, a blood-born tumor such as acute lymphoblastic leukemia, acute lymphoblastic B-cell leukemia, acute lymphoblastic T-cell leukemia, acute myeloblastic leukemia, acute promyelocytic leukemia, acute monoblastic leukemia, acute erythroleukemic leukemia, acute megakaryoblastic leukemia, acute myelomonocytic leukemia, acute nonlymphocyctic leukemia, acute undifferentiated leukemia, chronic myelocytic leukemia, chronic lymphocytic leukemia, hairy cell leukemia, or multiple myeloma. See e.g., Harrison's Principles of Internal Medicine, Eugene Braunwald et al., eds., pp. 491-762 (15th ed. 2001).
In yet another embodiment, the invention encompasses the treatment of a human afflicted with a solid tumor or a blood tumor.
In a preferred embodiment, the invention encompasses a method of treating or preventing a disease ameliorated by modulation of premature translation termination, nonsense-mediated mRNA decay, or premature translation termination and nonsense-mediated mRNA decay, or ameliorating one or more symptoms associated therewith comprising contacting a cell with a therapeutically effective amount of a compound of the invention. Cells encompassed by the present methods include animal cells, mammalian cells, bacterial cells, and virally infected cells. In one embodiment, the nonsense mutation is a genetic mutation (i.e., the nonsense codon was present in the progenitor DNA). In another embodiment, the nonsense mutation is a somatic mutation (i.e., the nonsense codon arose spontaneously or from mutagenesis).
In certain embodiments, a compound of the invention is administered to a subject, including but not limited to a plant, reptile, avian, amphibian or preferably a mammal, more preferably a human, as a preventative measure against a disease associated with premature translation termination, nonsense-mediated mRNA decay, or premature translation termination and nonsense-mediated mRNA decay.
In a preferred embodiment, it is first determined that the patient is suffering from a disease associated with premature translation termination and/or nonsense-mediated mRNA decay. In another embodiment, the patient has undergone a screening process to determine the presence of a nonsense mutation comprising the steps of screening a subject, or cells extracted therefrom, by an acceptable nonsense mutation screening assay. In a preferred embodiment, the DNA of the patient can be sequenced or subjected to Southern Blot, polymerase chain reaction (PCR), use of the Short Tandem Repeat (STR), or polymorphic length restriction fragments (RFLP) analysis to determine if a nonsense mutation is present in the DNA of the patient. In one embodiment, it is determined whether the nonsense mutation is a genetic mutation or a somatic mutation by comparison of progenitor DNA. Alternatively, it can be determined if altered levels of the protein with the nonsense mutation are expressed in the patient by western blot or other immunoassays. In another embodiment, the patient is an unborn child who has undergone screening in utero for the presence of a nonsense mutation. Administration of a compound of the invention can occur either before or after birth. In a related embodiment, the therapy is personalized in that the patient is screened for a nonsense mutation screening assay and treated by the administration of one or more compounds of the invention; particularly, the patient may be treated with a compound particularly suited for the mutations in question; e.g., depending upon the disease type, cell type, and the gene in question. Such methods are well known to one of skill in the art.
In another embodiment, the cells (e.g., animal cells, mammalian cells, bacterial cells, plant cells and virally infected cells) are screened for premature translation termination and/or nonsense-mediated mRNA decay with a method such as that described above (i.e., the DNA of the cell can be sequenced or subjected to Southern Blot, polymerase chain reaction (PCR), use of the Short Tandem Repeat (STR), or polymorphic length restriction fragments (RFLP) analysis to determine if a nonsense mutation is present in the DNA of the cell; the RNA of the cell can be subjected to quantitative real time PCR to determine transcript abundance).
Specific methods of the invention further comprise the administration of an additional therapeutic agent (i.e., a therapeutic agent other than a compound of the invention). In certain embodiments of the present invention, the compounds of the invention can be used in combination with at least one other therapeutic agent. Therapeutic agents include, but are not limited to non-opioid analgesics; non-steroid anti-inflammatory agents; steroids, antiemetics; β-adrenergic blockers; anticonvulsants; antidepressants; Ca2+-channel blockers; anticancer agent(s) and antibiotics and mixtures thereof.
In certain embodiments, the compounds of the invention can be administered or formulated in combination with anticancer agents. Suitable anticancer agents include, but are not limited to: alkylating agents; nitrogen mustards; folate antagonists; purine antagonists; pyrimidine antagonists; spindle poisons; topoisomerase inhibitors; apoptosis inducing agents; angiogenesis inhibitors; podophyllotoxins; nitrosoureas; cisplatin; carboplatin; interferon; asparginase; tamoxifen; leuprolide; flutamide; megestrol; mitomycin; bleomycin; doxorubicin; irinotecan and taxol.
In certain embodiments, the compounds of the invention can be administered or formulated in combination with antibiotics. In certain embodiments, the antibiotic is an aminoglycoside (e.g., tobramycin), a cephalosporin (e.g., cephalexin, cephradine, cefuroxime, cefprozil, cefaclor, cefixime or cefadroxil), a clarithromycin (e.g., clarithromycin), a macrolide (e.g., erythromycin), a penicillin (e.g., penicillin V) or a quinolone (e.g., ofloxacin, ciprofloxacin or norfloxacin). In a preferred embodiment, the antibiotic is active against Pseudomonas aeruginosa.
Without intending to be limited by theory, it is believed that the methods of the present invention act through a combination of mechanisms that suppress nonsense mutations. In preferred embodiments, the methods of the invention comprise administering a therapeutically effective amount of at least one compound of the invention, e.g., a compound of Formula 1. Relative activity of the compounds of the invention may be determined by any method known in the art, including the assay described in Example 2 herein.
Compounds of the invention can be characterized with an in vitro luciferase nonsense suppression assay. Luciferase assays are included in the methods of the present invention. Luciferase can be used as a functional reporter gene assay (light is only produced if the protein is functional), and luciferase is extremely sensitive (Light intensity is proportional to luciferase concentration in the nM range). In one embodiment, an assay of the present invention is a cell-based luciferase reporter assay. In a preferred cell-based luciferase reporter assay, a luciferase reporter construct containing a premature termination codon (UGA, UAA, or UAG) is stably transfected in 293 Human Embryonic Kidney cells.
In another assay of the present invention, a preferred assay is a biochemical assay consisting of rabbit reticulocyte lysate and a nonsense-containing luciferase reporter mRNA. In another assay of the present invention, the assay is a biochemical assay consisting of prepared and optimized cell extract (Lie & Macdonald, 1999, Development 126(22):4989-4996 and Lie & Macdonald, 2000, Biochem. Biophys. Res. Commun. 270(2):473-481). In the biochemical assay, mRNA containing a premature termination codon (UGA, UAA, or UAG) is used as a reporter in an in vitro translation reaction using rabbit reticulocyte lysate supplemented with tRNA, hemin, creatine kinase, amino acids, KOAc, Mg(OAc)2, and creatine phosphate. Translation of the mRNA is initiated within a virus derived leader sequence, which significantly reduces the cost of the assay because capped RNA is not required. Synthetic mRNA is prepared in vitro using the T7 promoter and the MegaScript in vitro transcription kit (Ambion, Inc.; Austin, Tex.). In assays of the present invention, addition of gentamicin, an aminoglycoside known to allow readthrough of premature termination codons, results in increased luciferase activity and can be used as an internal standard. Assays of the present invention can be used in high-throughput screens. Hundreds of thousands of compounds can be screened in cell-based and biochemical assays of the present invention. In a preferred aspect, a functional cell-based assay similar to the one described.
Compounds of the present invention include compounds capable of increasing specific, functional protein expression from mRNA molecules comprising premature termination codons. In one embodiment, compounds of the present invention can preferentially suppress premature translation termination. For example, a compound of the present invention can be capable of suppressing a nonsense mutation if the mutation results in UAA, but not capable of suppressing a nonsense mutation if the mutation results in UAG. Another non-limiting example can occur when a compound of the present invention can be capable of suppressing a nonsense mutation if the mutation results in UAA and is followed, in-frame by a cytosine at the +1 position, but not capable of suppressing a nonsense mutation if the mutation results in UAA and is followed, in-frame by an adenine at the +1 position.
A stable cell line harboring the UGA nonsense-containing luciferase gene can be treated with a test compound. In this aspect, cells can be grown in standard medium supplemented with 1% penicillin-streptomycin (P/S) and 10% fetal bovine serum (FBS) to 70% confluency and split 1:1 the day before treatment. The next day, cells are trypsinized and 40,000 cells are added to each well of a 96-well tissue culture dish. Serial dilutions of each compound are prepared to generate a six-point dose response curve spanning 2 logs (30 μM to 0.3 μM). The final concentration of the DMSO solvent remains constant at 1% in each well. Cells treated with 1% DMSO serve as the background standard, and cells treated with gentamicin serve as a positive control.
To address the effects of the nonsense-suppressing compounds on mRNAs altered in specific inherited diseases, a bronchial epithelial cell line harboring a nonsense codon at amino acid 1282 (W1282X) can be treated with a compound of the invention and CFTR function is monitored as a cAMP-activated chloride channel using the SPQ assay (Yang et al., Hum. Mol. Genet. 2(8):1253-1261 (1993) and Howard et al., Nat. Med. 2(4):467-469 (1996)). The increase in SPQ fluorescence in cells treated with a compound of the invention is compared to those treated with cAMP and untreated cells. An increase in SPQ fluorescence in cells is consistent with stimulation of CFTR-mediated halide efflux and an increase in readthrough of the nonsense codon. Full-length CFTR expression from this nonsense-containing allele following treatment with a compound of the invention demonstrates that cystic fibrosis cell lines increase chloride channel activity when treated with a compound of the invention.
D. Metabolites of the Compounds of the Invention
Also falling within the scope of the present invention are the in vivo metabolic products of the compounds described herein. Such products may result for example from the oxidation, reduction, hydrolysis, amidation, esterification and the like of the administered compound, primarily due to enzymatic processes. Accordingly, the invention includes compounds produced by a process comprising contacting a compound of this invention with a mammalian tissue or a mammal for a period of time sufficient to yield a metabolic product thereof. Such products typically are identified by preparing a radio-labeled (e.g. C14 or H3) compound of the invention, administering it in a detectable dose (e.g., greater than about 0.5 mg/kg) to a mammal such as rat, mouse, guinea pig, monkey, or to man, allowing sufficient time for metabolism to occur (typically about 30 seconds to 30 hours), and isolating its conversion products from urine, blood or other biological samples. These products are easily isolated since they are labeled (others are isolated by the use of antibodies capable of binding epitopes surviving in the metabolite). The metabolite structures are determined in conventional fashion, e.g., by MS or NMR analysis. In general, analysis of metabolites may be done in the same way as conventional drug metabolism studies well-known to those skilled in the art. The conversion products, so long as they are not otherwise found in vivo, are useful in diagnostic assays for therapeutic dosing of the compounds of the invention even if they possess no biological activity of their own.
E. Pharmaceutical Compositions of the Invention
While it is possible for the compounds of the present invention to be administered neat, it may be preferable to formulate the compounds as pharmaceutical compositions. As such, in yet another aspect of the invention, pharmaceutical compositions useful in the methods of the invention are provided. The pharmaceutical compositions of the invention may be formulated with pharmaceutically acceptable excipients such as carriers, solvents, stabilizers, adjuvants, diluents, etc., depending upon the particular mode of administration and dosage form. The pharmaceutical compositions should generally be formulated to achieve a physiologically compatible pH, and may range from a pH of about 3 to a pH of about 11, preferably about pH 3 to about pH 7, depending on the formulation and route of administration. In another preferred embodiment, the pharmaceutical compositions of the present invention may be formulated from about pH 4 to about pH 7. In alternative embodiments, it may be preferred that the pH is adjusted to a range from about pH 5 to about pH 8.
More particularly, the pharmaceutical compositions of the invention comprise a therapeutically or prophylactically effective amount of at least one compound of the present invention, together with one or more pharmaceutically acceptable excipients. Optionally, the pharmaceutical compositions of the invention may comprise a combination of compounds of the present invention, or may include a second active ingredient useful in the treatment of cancer, diabetic retinopathy, or exudative macular degeneration.
Formulations of the present invention, e.g., for parenteral or oral administration, are most typically solids, liquid solutions, emulsions or suspensions, while inhalable formulations for pulmonary administration are generally liquids or powders, with powder formulations being generally preferred. A preferred pharmaceutical composition of the invention may also be formulated as a lyophilized solid that is reconstituted with a physiologically compatible solvent prior to administration. Alternative pharmaceutical compositions of the invention may be formulated as syrups, creams, ointments, tablets, and the like.
The pharmaceutical compositions of the invention can be administered to the subject via any drug delivery route known in the art. Specific exemplary administration routes include oral, ocular, rectal, buccal, topical, nasal, ophthalmic, subcutaneous, intramuscular, intravenous (bolus and infusion), intracerebral, transdermal, and pulmonary.
The term “pharmaceutically acceptable excipient” refers to an excipient for administration of a pharmaceutical agent, such as the compounds of the present invention. The term refers to any pharmaceutical excipient that may be administered without undue toxicity. Pharmaceutically acceptable excipients are determined in part by the particular composition being administered, as well as by the particular method used to administer the composition. Accordingly, there exists a wide variety of suitable formulations of pharmaceutical compositions of the present invention (see, e.g., Remington's Pharmaceutical Sciences, 18th Ed., Mack Publishing Co., 1990).
Suitable excipients may be carrier molecules that include large, slowly metabolized macromolecules such as proteins, polysaccharides, polylactic acids, polyglycolic acids, polymeric amino acids, amino acid copolymers, and inactive virus particles. Other exemplary excipients include antioxidants such as ascorbic acid; chelating agents such as EDTA; carbohydrates such as dextrin, hydroxyalkylcellulose, hydroxyalkylmethylcellulose, stearic acid; liquids such as oils, water, saline, glycerol and ethanol; wetting or emulsifying agents; pH buffering substances; and the like. Liposomes are also included within the definition of pharmaceutically acceptable excipients.
The pharmaceutical compositions of the invention may be formulated in any form suitable for the intended method of administration. When intended for oral use for example, tablets, troches, lozenges, aqueous or oil suspensions, non-aqueous solutions, dispersible powders or granules (including micronized particles or nanoparticles), emulsions, hard or soft capsules, syrups or elixirs may be prepared. Compositions intended for oral use may be prepared according to any method known to the art for the manufacture of pharmaceutical compositions, and such compositions may contain one or more agents including sweetening agents, flavoring agents, coloring agents and preserving agents, in order to provide a palatable preparation.
Pharmaceutically acceptable excipients particularly suitable for use in conjunction with tablets include, for example, inert diluents, such as celluloses, calcium or sodium carbonate, lactose, calcium or sodium phosphate; disintegrating agents, such as croscarmellose sodium, cross-linked povidone, maize starch, or alginic acid; binding agents, such as povidone, starch, gelatin or acacia; and lubricating agents, such as magnesium stearate, stearic acid or talc. Tablets may be uncoated or may be coated by known techniques including microencapsulation to delay disintegration and adsorption in the gastrointestinal tract and thereby provide a sustained action over a longer period. For example, a time delay material such as glyceryl monostearate or glyceryl distearate alone or with a wax may be employed.
Formulations for oral use may be also presented as hard gelatin capsules where the active ingredient is mixed with an inert solid diluent, for example celluloses, lactose, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with non-aqueous or oil medium, such as glycerin, propylene glycol, polyethylene glycol, peanut oil, liquid paraffin or olive oil.
In another embodiment, pharmaceutical compositions of the invention may be formulated as suspensions comprising a compound of the present invention in admixture with at least one pharmaceutically acceptable excipient suitable for the manufacture of a suspension. In yet another embodiment, pharmaceutical compositions of the invention may be formulated as dispersible powders and granules suitable for preparation of a suspension by the addition of suitable excipients.
Excipients suitable for use in connection with suspensions include suspending agents, such as sodium carboxymethylcellulose, methylcellulose, hydroxypropyl methylcelluose, sodium alginate, polyvinylpyrrolidone, gum tragacanth, gum acacia, dispersing or wetting agents such as a naturally occurring phosphatide (e.g., lecithin), a condensation product of an alkylene oxide with a fatty acid (e.g., polyoxyethylene stearate), a condensation product of ethylene oxide with a long chain aliphatic alcohol (e.g., heptadecaethyleneoxycethanol), a condensation product of ethylene oxide with a partial ester derived from a fatty acid and a hexitol anhydride (e.g., polyoxyethylene sorbitan monooleate); and thickening agents, such as carbomer, beeswax, hard paraffin or cetyl alcohol. The suspensions may also contain one or more preservatives such as acetic acid, methyl and/or n-propyl p-hydroxy-benzoate; one or more coloring agents; one or more flavoring agents; and one or more sweetening agents such as sucrose or saccharin.
The pharmaceutical compositions of the invention may also be in the form of oil-in-water emulsions. The oily phase may be a vegetable oil, such as olive oil or arachis oil, a mineral oil, such as liquid paraffin, or a mixture of these. Suitable emulsifying agents include naturally-occurring gums, such as gum acacia and gum tragacanth; naturally occurring phosphatides, such as soybean lecithin, esters or partial esters derived from fatty acids; hexitol anhydrides, such as sorbitan monooleate; and condensation products of these partial esters with ethylene oxide, such as polyoxyethylene sorbitan monooleate. The emulsion may also contain sweetening and flavoring agents. Syrups and elixirs may be formulated with sweetening agents, such as glycerol, sorbitol or sucrose. Such formulations may also contain a demulcent, a preservative, a flavoring or a coloring agent.
Additionally, the pharmaceutical compositions of the invention may be in the form of a sterile injectable preparation, such as a sterile injectable aqueous emulsion or oleaginous suspension. This emulsion or suspension may be formulated according to the known art using those suitable dispersing or wetting agents and suspending agents which have been mentioned above. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, such as a solution in 1,2-propane-diol. The sterile injectable preparation may also be prepared as a lyophilized powder. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, and isotonic sodium chloride solution. In addition, sterile fixed oils may be employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid may likewise be used in the preparation of injectables.
Generally, the compounds of the present invention useful in the methods of the present invention are substantially insoluble in water and are sparingly soluble in most pharmaceutically acceptable protic solvents and in vegetable oils. However, the compounds are generally soluble in medium chain fatty acids (e.g., caprylic and capric acids) or triglycerides and have high solubility in propylene glycol esters of medium chain fatty acids. Also contemplated in the invention are compounds which have been modified by substitutions or additions of chemical or biochemical moieties which make them more suitable for delivery (e.g., increase solubility, bioactivity, palatability, decrease adverse reactions, etc.), for example by esterification, glycosylation, PEGylation, etc.
In a preferred embodiment, the compounds of the present invention may be formulated for oral administration in a lipid-based formulation suitable for low solubility compounds. Lipid-based formulations can generally enhance the oral bioavailability of such compounds. As such, a preferred pharmaceutical composition of the invention comprises a therapeutically or prophylactically effective amount of a compound of the present invention, together with at least one pharmaceutically acceptable excipient selected from the group consisting of: medium chain fatty acids or propylene glycol esters thereof (e.g., propylene glycol esters of edible fatty acids such as caprylic and capric fatty acids) and pharmaceutically acceptable surfactants such as polyoxyl 40 hydrogenated castor oil.
In an alternative preferred embodiment, cyclodextrins may be added as aqueous solubility enhancers. Preferred cyclodextrins include hydroxypropyl, hydroxyethyl, glucosyl, maltosyl and maltotriosyl derivatives of α-, β-, and γ-cyclodextrin. A particularly preferred cyclodextrin solubility enhancer is hydroxypropyl-β-cyclodextrin (HPBC), which may be added to any of the above-described compositions to further improve the aqueous solubility characteristics of the compounds of the present invention. In one embodiment, the composition comprises 0.1% to 20% hydroxypropyl-β-cyclodextrin, more preferably 1% to 15% hydroxypropyl-β-cyclodextrin, and even more preferably from 2.5% to 10% hydroxypropyl-β-cyclodextrin. The amount of solubility enhancer employed will depend on the amount of the compound of the present invention in the composition.
The therapeutically effective amount, as used herein, refers to an amount of a pharmaceutical composition of the invention to treat, ameliorate, or modulate an identified disease or condition, or to exhibit a detectable therapeutic or inhibitory effect. The effect can be detected by, for example, assays of the present invention. The effect can also be the prevention of a disease or condition where the disease or condition is predicted for an individual or a high percentage of a population.
The precise effective amount for a subject will depend upon the subject's body weight, size, and health; the nature and extent of the condition; the therapeutic or combination of therapeutics selected for administration, the protein half-life, the mRNA half-life and the protein localization. Therapeutically effective amounts for a given situation can be determined by routine experimentation that is within the skill and judgment of the clinician.
For any compound, the therapeutically effective amount can be estimated initially either in cell culture assays, e.g., of neoplastic cells, or in animal models, usually rats, mice, rabbits, dogs, or pigs. The animal model may also be used to determine the appropriate concentration range and route of administration. Such information can then be used to determine useful doses and routes for administration in humans. Therapeutic/prophylactic efficacy and toxicity may be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., ED50 (the dose therapeutically effective in 50% of the population) and LD50 (the dose lethal to 50% of the population). The dose ratio between toxic and therapeutic effects is the therapeutic index, and it can be expressed as the ratio, LD50/ED50. Pharmaceutical compositions that exhibit large therapeutic indices are preferred. The data obtained from cell culture assays and animal studies may be used in formulating a range of dosage for human use. The dosage contained in such compositions is preferably within a range of circulating concentrations that include an ED50 with little or no toxicity. The dosage may vary within this range depending upon the dosage form employed, sensitivity of the patient, and the route of administration.
More specifically, the concentration-biological effect relationships observed with regard to the compound(s) of the present invention indicate an initial target plasma concentration ranging from approximately 5 μg/mL to approximately 100 μg/mL, preferably from approximately 10 μg/mL to approximately 50 μg/mL, more preferably from approximately 10 μg/mL to approximately 25 μg/mL. To achieve such plasma concentrations, the compounds of the invention may be administered at doses that vary from 1 mg/kg to 150 mg/kg, depending upon the route of administration. Guidance as to particular dosages and methods of delivery is provided in the literature and is generally available to practitioners in the art. In general the dose will be in the range of about 1 mg/day to about 10 g/day, or about 0.1 g to about 3 g/day, or about 0.3 g to about 3 g/day, or about 0.5 g to about 2 g/day, in single, divided, or continuous doses for a patient weighing between about 40 to about 100 kg (which dose may be adjusted for patients above or below this weight range, particularly children under 40 kg).
The magnitude of a prophylactic or therapeutic dose of a particular active ingredient of the invention in the acute or chronic management of a disease or condition will vary, however, with the nature and severity of the disease or condition, and the route by which the active ingredient is administered. The dose, and perhaps the dose frequency, will also vary according to the age, body weight, and response of the individual patient. Suitable dosing regimens can be readily selected by those skilled in the art with due consideration of such factors. In general, the recommended daily dose range for the conditions described herein lie within the range of from about 1 mg/kg to about 150 mg/kg per day. In one embodiment, the compound of the invention is given as a single once-a-day dose. In another embodiment, the compound of the invention is given as divided doses throughout a day. More specifically, the daily dose is administered in a single dose or in equally divided doses. Preferably, a daily dose range should be from about 5 mg/kg to about 100 mg/kg per day, more preferably, between about 10 mg/kg and about 90 mg/kg per day, even more preferably 20 mg/kg to 60 mg/kg per day. In managing the patient, the therapy should be initiated at a lower dose, perhaps about 200 mg to about 300 mg, and increased if necessary up to about 600 mg to about 4000 mg per day as either a single dose or divided doses, depending on the patient's global response. It may be necessary to use dosages of the active ingredient outside the ranges disclosed herein in some cases, as will be apparent to those of ordinary skill in the art. Furthermore, it is noted that the clinician or treating physician will know how and when to interrupt, adjust, or terminate therapy in conjunction with individual patient response.
As stated above, different therapeutically effective amounts may be applicable for different diseases and conditions, as will be readily known by those of ordinary skill in the art. Similarly, amounts sufficient to treat or prevent such diseases, but insufficient to cause, or sufficient to reduce, adverse effects associated with conventional therapies are also encompassed by the above described dosage amounts and dose frequency schedules.
The exact dosage will be determined by the practitioner, in light of factors related to the subject that requires treatment. Dosage and administration are adjusted to provide sufficient levels of the active agent(s) or to maintain the desired effect. Factors which may be taken into account include the severity of the disease state, general health of the subject, age, weight, and gender of the subject, diet, time, protein of interest half-life, RNA of interest half-life, frequency of administration, drug combination(s), reaction sensitivities, and tolerance/response to therapy. Long-acting pharmaceutical compositions may be administered every 3 to 4 days, every week, or once every two weeks depending on half-life and clearance rate of the particular formulation.
F. Combination Therapy
It is also possible to combine any compound of the present invention with one or more other active ingredients useful in the treatment of diseases associated with nonsense mutations of mRNA as described herein, including compounds in a unitary dosage form, or in separate dosage forms intended for simultaneous or sequential administration to a patient in need of treatment. When administered sequentially, the combination may be administered in two or more administrations. In an alternative embodiment, it is possible to administer one or more compounds of the present invention and one or more additional active ingredients by different routes.
The skilled artisan will recognize that a variety of active ingredients may be administered in combination with the compounds of the present invention that may act to augment or synergistically enhance the nonsense mutation-suppressing activity of the compounds of the invention.
According to the methods of the invention, the combination of active ingredients may be: (1) co-formulated and administered or delivered simultaneously in a combined formulation; (2) delivered by alternation or in parallel as separate formulations; or (3) by any other combination therapy regimen known in the art. When delivered in alternation therapy, the methods of the invention may comprise administering or delivering the active ingredients sequentially, e.g., in separate solution, emulsion, suspension, tablets, pills or capsules, or by different injections in separate syringes. In general, during alternation therapy, an effective dosage of each active ingredient is administered sequentially, i.e., serially, whereas in simultaneous therapy, effective dosages of two or more active ingredients are administered together. Various sequences of intermittent combination therapy may also be used.
G. Gene Therapy
The compounds of the present invention or other nonsense compounds can be utilized in combination with gene therapy. In this embodiment, a gene can be introduced or provided to a mammal, preferably a human that contains a specified nonsense mutation in the desired gene. In a preferred aspect, the desired gene is selected from the group consisting of IGF1, EPO, p53, p19ARF, p21, PTEN, EI 24 and ApoAI. In order to obtain expression of the full-length polypeptide in a patient or mammal, the patient or mammal would be provided with an effective amount of a compound of the present invention or other nonsense suppression compound when such polypeptide is desired.
There are two major approaches to getting nucleic acid that contain a nonsense mutation (optionally contained in a vector) into the patient's cells: in vivo and ex vivo. For in vivo delivery the nucleic acid is injected directly into the patient, usually at the sites where the polypeptide is required, i.e., the site of synthesis of the polypeptide, if known, and the site (e.g. solid tumor) where biological activity of the polypeptide is needed. For ex vivo treatment, the patient's cells are removed, the nucleic acid is introduced into these isolated cells, and the modified cells are administered to the patient either directly or, for example, encapsulated within porous membranes that are implanted into the patient (see e.g., U.S. Pat. Nos. 4,892,538 and 5,283,187). There are a variety of techniques available for introducing nucleic acids into viable cells. The techniques vary depending upon whether the nucleic acid is transferred into cultured cells in vitro, or transferred in vivo in the cells of the intended host. Techniques suitable for the transfer of nucleic acid into mammalian cells in vitro include the use of liposomes, electroporation, microinjection, transduction, cell fusion, DEAE-dextran, the calcium phosphate precipitation method, etc. Transduction involves the association of a replication-defective, recombinant viral (preferably retroviral) particle with a cellular receptor, followed by introduction of the nucleic acids contained by the particle into the cell. A commonly used vector for ex vivo delivery of the gene is a retrovirus.
The currently preferred in vivo nucleic and transfer techniques include transfection with viral or non-viral vectors (such as adenovirus, lentivirus, Herpes simplex I virus, or adeno-associated virus (AAV)) and lipid-based systems (useful lipids for lipid-mediated transfer of the gene are, for example, DOTMA, DOPE, and DC-Chol; see, e.g., Tonkinson et al., Cancer Investigation, 14 (1): 54-65 (1996)). The most preferred vectors for use in gene therapy are viruses, most preferably adenoviruses, AAV, lentiviruses, or retroviruses. A viral vector such as a retroviral vector includes at least one transcriptional promoter/enhancer or locus-defining element(s), or other elements that control gene expression by other means such as alternate splicing, nuclear RNA export, or post-translational modification of messenger. In addition, a viral vector such as a retroviral vector includes a nucleic acid molecule that, when transcribed with a gene encoding a polypeptide, is operably linked to the coding sequence and acts as a translation initiation sequence. Such vector constructs also include a packaging signal, long terminal repeats (LTRs) or portions thereof, and positive and negative strand primer binding sites appropriate to the virus used (if these are not already present in the viral vector). In addition, such vector typically includes a signal sequence for secretion of the polypeptide from a host cell in which it is placed. Preferably the signal sequence for this purpose is a mammalian signal sequence, most preferably the native signal sequence for the polypeptide. Optionally, the vector construct may also include a signal that directs polyadenylation, as well as one or more restriction sites and a translation termination sequences. By way of example, such vectors will typically include a 5′ LTR, a tRNA binding site, a packaging signal, a origin of second-strand DNA synthesis, and a 3′ LTR or a portion thereof. Other vectors can be used that are non-viral, such as cationic lipids, polylysine, and dendrimers.
In some situations, it is desirable to provide the nucleic acid source with an agent that targets the target cells, such as an antibody specific for a cell-surface membrane protein or the target cell, a ligand for a receptor on the target cell, etc. Where liposomes are employed, proteins that bind to a cell-surface membrane protein associated with endocytosis may be used for targeting and/or to facilitate uptake, e.g., capsid proteins or fragments thereof tropic for a particular cell type, antibodies for proteins that undergo internalization in cycling, and proteins that target intracellular localization and enhance intracellular half-life. The technique of recpto-mediated endocytosis is described, for example, by Wu et al., J. Biol. Chem. 262: 4429-4432 (1987); and Wagner et al., Proc. Natl. Acad. Sci. USA, 87: 3410-3414 (1990). For a review of the currently known gene marking and gene therapy protocols, see, Anderson et al., Science 256: 808-813 (1992). See also WO 93/25673 and the references cited therein.
Suitable gene therapy and methods for making retroviral particles and structural proteins can be found in, e.g. U.S. Pat. Nos. 5,681,746; 6,800,604 and 6,800,731.
To assist in understanding the present invention, the following Examples are included. The experiments relating to this invention should not, of course, be construed as specifically limiting the invention and such variations of the invention, now known or later developed, which would be within the purview of one skilled in the art are considered to fall within the scope of the invention as described herein and hereinafter claimed.
The present invention is described in more detail with reference to the following non-limiting examples, which are offered to more fully illustrate the invention, but are not to be construed as limiting the scope thereof. The examples illustrate the preparation of certain compounds of the invention, and the testing of these compounds in vitro and/or in vivo. Those of skill in the art will understand that the techniques described in these examples represent techniques described by the inventors to function well in the practice of the invention, and as such constitute preferred modes for the practice thereof. However, it should be appreciated that those of skill in the art should in light of the present disclosure, appreciate that many changes can be made in the specific methods that are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.
3-(6-methyl-benzooxazol-2-yl)-benzoic acid (Compound 3) and similar compounds of the invention may be generally prepared according to Scheme A as follows.
A solution of 3-cyanobenzoic acid (3.15 g, 21.41 mmol) and K2CO3 (4.85 g, 35.48 mmol) in DMF (30 ml) is treated with iodomethane (4.56 g, 32.11 mmol) and stirred at room temperature for 5 h until the complete consumption of the starting material. The reaction mixture is poured into 120 ml of ice-water to precipitate solid. The solid is recrystallized from 100 ml of water-methanol to provide 2.6 g (75.3% yield) of the product as a white crystalline solid; 1H NMR (300 MHz, CDCl3): δ 8.32 (t, 1H), δ 8.26 (td, J1=7.9, J2=1.7, 1H), δ 7.72 (td, J1=7.6, J2=1.7, 1H), δ 7.61 (dt, J1=7.7, J2=7.6, 1H), δ 3.96 (s, 3H); MS+=162.
3-Cyano-benzoic acid methyl ester (0.51 g, 3.17 mmol) is dissolved in 10 ml of methanol, acetyl chloride (6.0 ml, 84.38 mmol) is added to the solution at room temperature under stirring. After 5˜6 h, the mixture is dried under reduced pressure to give a crude product which is washed with ethyl ether to obtain a pure product as white crystal flakes. The product is used immediately for the next step.
A mixture of 3-methoxycarboniumidoyl-benzoic acid methyl ester hydrochloride (II) and 2-amino-5-methyl phenol (0.39 g, 3.17 mmol) in 12.0 ml of methanol is refluxed for 4 h. Methanol is evaporated. The residue is purified by flash chromatography using a solvent mixture (ethyl acetate/hexanes=1:20) to afford 3-(6-methyl-benzooxazol-2-yl)-benzoic acid methyl ester (0.31 g, 36.9%) as a white solid; 1H NMR (300 MHz, CDCl3): δ 8.88 (t, 1H), δ 8.34 (td, J1=7.8, J2=1.8, 1H), δ 8.18 (td, J1=8.1, J2=1.5, 1H), δ 7.62 (m, 2H), δ 7.40 (s, 1H), 7.21 (dd, J1=7.2, J2=1.5, 1H), δ 3.99 (s, 3H), δ 2.53 (s, 3H); ES+=268.
A suspension of 3-(6-methyl-benzooxazol-2-yl)-benzoic acid methyl ester (0.21 g, 0.78 mmol) and lithium iodide (1.05 g, 7.84 mmol) in 4.0 ml of dry pyridine is refluxed for 5 h until invisible starting material by TLC. 1N HCl is added to the reaction mixture until PH<7. The resulting acidic mixture is extracted with ethyl acetate (2×10.0 ml). The combined ethyl acetate is dried over Mg2SO4, and evaporated under reduced pressure to give the crude product. The crude product is recrystallized from 8.0 ml of methanol to provide 50.0 mg (25.1% yield) as the white powder. Mp: 239-241° C.; 1H NMR (300 MHz, DMSO-d6): δ 13.36 (s, 1H), δ 8.65 (t, 1H), δ 8.35 (td, J1=6.1, J2=1.5, 1H), δ 8.11 (td, J1=7.4, J2=1.2, 1H), δ 7.68 (m, 2H), δ 7.59 (s, 1H), δ 7.24 (d, J=7.8, 1H), δ 2.46 (overlapping with DMSO-d6, 3H); ES+=254.
3-(5-p-Tolylbenzoxazol-2-yl)benzoic acid and similar compounds of the invention may generally be prepared according to Scheme B as follows.
In a 10 ml glass tube are placed 3-(5-bromo-benzooxazole-2-yl)benzoic acid methyl ester (508.0 mg, 1.53 mmol), 4-methyl-phenylboronic acid (207.9 mg, 1.53 mmol), Na2CO3 (479.0 mg, 4.56 mmol), t-butylammonia iodide (565.0 mg, 1.53 mmol), 6 ml of H2O, and a stirring bar. The vessel is sealed and placed into the microwave cavity. 60 w of power and 150° C. is used for the reaction condition. The reaction is held for 10 min. and detected by LC-MS for the complete conversion of the starting materials to the desired product. The reaction mixture is acidified using 1N HCl until PH<7, and partitioned between ethyl acetate and water. Water layer is extracted with ethyl acetate (3×15 ml). Ethyl acetate is combined and washed with Brine, solid is crushed out in organic phase. Ethyl acetate is removed by reduce pressure. The residue is washed with water followed by ethyl ether to afford the desired product as a white crystalline solid. The obtained compound is >95% pure as determined by LC-MS. Mp: 305-308° C. 1H NMR (300 MHz, DMSO-d6): δ 8.74 (s, 1H), δ 8.16 (d, J=3.8, 1H), δ 8.11 (d, J=3.8, 1H), δ 8.00 (d, J=1.5, 1H), δ 7.83 (d, J=8.6, 1H), δ 7.66 (dd, J1=8.6, J2=1.8, 1H), δ 7.61 (d, J=8.1, 2H), δ 7.54 (dt, J1=7.6, J2=7.4, 1H), δ 7.27 (d, J=8.1, 2H), δ 2.37 (s, 3H); ES+=330.
3-[5-(2-Oxo-pyrrolidin-1-yl)-benzoxazol-2-yl]-benzoic acid (Compound 66), 3-[5-(Pyrrolidin-1-yl)-benzoxazol-2-yl]-benzoic acid (Compound 42), and similar compounds of the invention may be generally prepared according to Scheme C as follows.
A 50 ml culture tube is placed with 3-(5-bromo-benzooxazole-2-yl)benzoic acid methyl ester (478.5 mg, 1.44 mmol), CuI (13.7 mg, 0.72 mmol.), pyrrolidin-2-one (153.3 mg, 1.80 mmol.), and K2CO3 (398.2 mg, 2.88 mmol), evacuated, and backed charged with N2. Trans-diamino-cyclohexane (16.4 mg, 0.14 mmol) and toluene (3.0 ml) are added under N2. The tube is sealed with a Teflon cap and the reaction mixture is stirred at 110° C. for 15 h. The resulting reaction mixture is added water, and extracted with ethyl acetate. The organic layer is washed with H2O to afford a pink solid which is purified by flash chromatography using a mixture of ethyl acetate-hexanes (1:10) followed by methanol-methylene chloride (1:20) to provide 238.0 mg desired product as a light-brown solid.
A suspension of the above product (202.1 mg, 0.60 mmol) in 3.0 ml of pyridine is added with LiI (1.61 g, 12.0 mmol) and refluxed overnight. TLC shows completion of the reaction. Addition of 1N HCl to the resulting solution obtains a brown solid as a crude product. The crude product is purified by a 2 g of Sped-ed PSA Pri/Sed Amine cartridge using a mixture of methanol-methylene chloride (1:10) as a solvent and being cleaved by a mixture of TFA-methylene chloride (1:5) to give 101.2 mg desired compound as a white solid. The obtained compound is >95% pure as determined by LC-MS. Mp: 190-192° C. 1H NMR (300 MHz, DMSO-d6): δ 13.37 (s, 1H), δ 8.68 (t, 1H), δ 8.37 (td, J=8.3, J=1.2, 1H), δ 8.15 (td, J1=7.6, J2=1.5, 1H), δ 8.03 (q, 1H), δ 7.76 (m, 3H), δ 3.91 (t, 2H), δ 2.50 (overlapping with DMSO-d6, 2H), 62.11 (m, 2H); ES+=323.
A mixture of methyl 3-carbomethoxybenzimidate hydrochloride (prepared from 0.72 g of methyl 3-cyanobenzoate) and 2-amino-5-(pyrrolidin-1-yl)phenol (0.79 g, 4.48 mmol) in 15 mL of methanol is refluxed for 4 h. Methanol is evaporated, and the residue is purified by flash chromatography (1:20 ethyl acetate/hexanes) to afford the title product (0.29 g, 20%) as a white solid. MS (ES+): m/z 323.
A suspension of methyl 3-[5-(pyrrolidin-1-yl)-benzoxazol-2-yl]-benzoate (74.3 mg, 0.23 mmol) and lithium iodide (309.1 g, 2.31 mmol) in 4 mL of anhydrous pyridine is refluxed for 5 h until the starting material is seen to be consumed by TLC. 1N HCl is added to the reaction mixture until pH<7. The resulting acidic mixture is extracted with ethyl acetate (2×10 mL). The combined ethyl estate is dried over Mg2SO4, and evaporated under reduced pressure to give the crude product. The crude product is recrystallized from 8 mL of methanol to provide 48.3 mg (31% yield) as a white powder, m.p. 248-250° C. 1H NMR (300 MHz, DMSO-d6): δ 13.39 (1H, s), 8.65 (1H, s), 8.33 (1H, dd, J=7.5, 0.9 Hz), 8.11 (1H, dd, J=7.8, 0.9 Hz), 7.78 (1H, d, J=8.7 Hz), 7.71 (1H, t, J=7.8 Hz), 6.82 (1H, s), 6.67 (1H, d, J=9.0 Hz), 3.38 (4H, m), 2.08 (4H, m). MS (ES+): m/z 309.
4-(5-Methoxybenzo[d]isoxazol-3-yl)-benzoic acid (Compound 125) and similar compounds of the invention may be generally prepared according to Schemes D and E as follows.
A mixture of 5-fluoro-2-nitrophenol (0.67 g, 4.26 mmol), pyrrolidine (0.84 g, 12.9 mmol) in DMSO (8.0 ml) is charged in a 50 ml culture tube and stirred at room temperature to 98° C. for 5 h. Yellow solid is precipitated by addition of water. 0.80 g (84.4% yield) of the desired product is collected by filtration and washed with water, hexanes in sequence. The obtained compound is >90% pure as determined by 1H NMR and LC-MS.
The obtained product from the above reaction (0.61 g, 2.74 mmol) is dissolved in methanol (30 ml), and Pd/C (122.5 mg, 20% by weight) is added to the reaction vessel. The mixture is shacked at room temperature using 55 psi hydrogen for 5-8 h until complete consumption of the starting material by TLC. Methanol is removed, and the residue is used for the next step (Scheme E) without purification.
4-Iodobenzoyl chloride (530 mg, 2 mmol) is dissolved in 1,2-dichloroethane (3 mL). 4-Isopropylanisole (320 μL, 2 mmol) is added, followed by aluminum chloride (280 mg, 1.1 mmol). This is stirred at rt overnight, and then at 80° C. for 3 h. The reaction mix is poured into ice water and this mixture is EtOAc-extracted. Purification by column (1:1 CH2Cl2:Hex) is done to yield product as a yellow oil (699 mg, 95% yield) with 3% 4-isopropylanisole impurity, which is carried through into the next reaction.
(2-Hydroxy-5-methoxy-phenyl)-(4-iodo-phenyl)-methanone (699 mg, 1.92 mmol), hydroxylamine hydrochloride (535 mg, 7.7 mmol), and pyridine (5 mL) are heated at 110° C. for 2 h. Pyridine is removed under reduced pressure. The residue is treated with dilute aqueous HCl, and this mixture is ether-extracted to yield oxime as an orange oil. This oxime is dissolved in DMF (7.2 mL). Sodium acetate (483 mg, 5.9 mmol) and acetic anhydride (550 μL, 5.9 mmol) is added. The reaction mixture is heated at 140° C. for 2 h. DMF and acetic anhydride is removed under reduced pressure. The residue is H2O-EtOAc extracted. Purification by column (1:1 CH2Cl2:Hex) is done to yield product as a white solid (330 mg, 47%).
3-(4-Iodo-phenyl)-5-methoxy-benzo[d]isoxazole (100 mg, 0.275 mmol) is dissolved in THF (650 μL) at 0° C. under N2. Isopropylmagnesium chloride (160 μL, 2 M in THF, 0.32 mmol) is added dropwise. After stirring for 30 min, the reaction mixture is quenched with solid CO2. The mixture is then acidified with dilute aqueous HCl and is ether-extracted. The ether layer is extracted with aqueous NaHCO3. This aqueous layer is acidified with dilute HCl and is EtOAc-extracted. Pure product is isolated as a white solid from the EtOAc layer (53 mg, 68%). 1H NMR (d-6 DMSO) σ: 1.25 (d, 6H), 3.08 (septet, 1H), 7.6 (dd, 1H), 7.72 (d, 1H), 7.88 (s, 1H), 8.08-8.16 (m, 4H); 13C NMR σ: 24.90, 34.17, 110.60, 119.64, 120.09, 128.71, 130.29, 130.83, 132.84, 132.96, 145.92, 156.47, 162.79, 167.35.
Similar compounds of the invention, such as Compounds 127, 128, 129, and 130, may be prepared in a similar manner.
3-(7,8-Dihydro-1,6,9-trioxa-2-aza-cyclopenta[a]napthalen-3-yl)-benzoic acid (Compound 132) and similar compounds of the invention may generally be prepared according to Scheme F as follows.
3-Iodobenzoyl chloride (6 mmol, prepared from 6 mmol 3-iodobenzoic acid in the standard way), is dissolved in 1,2-dichloroethane (9 ml) at 0° C. 1,2,3-Trimethoxybenzene (1.01 g, 6 mmol), and aluminum chloride (798 mg, 6 mmol) are added sequentially. This is stirred at rt overnight, and then at 60° C. for 2 h. The reaction mixture is poured into icy aqueous HCl, and this is then EtOAc-extracted. Purification by column (6:4 CH2Cl2:Hex) yields product as a yellow semisolid (1.733 g, 75%). This material has 7% 1,2,3-trimethoxybenzene impurity that is carried through the next reaction.
(2-Hydroxy-3,4-dimethoxy-phenyl)-(3-iodo-phenyl)-methanone (1.73 g, 4.5 mmol) is converted into oily product (892 mg, 52%) by a procedure similar to Scheme D, step 2. This product contains roughly 5% 1,2,3-trimethoxybenzene impurity that is carried through the next reaction.
3-(3-Iodo-phenyl)-6,7-dimethoxy-benzo[d]isoxazole (890 mg, 2.3 mmol) and pyridine hydrochloride (11.7 g, 101 mmol) are heated as a melt at 175° C. for 2 h. The mixture is cooled to rt, diluted in H2O, and is EtOAc-extracted. The EtOAc layer is back-washed with dilute HCl. Brown solid product (796 mg, 95%) is obtained from the EtOAc layer at roughly 85% purity, which is used as crude material in the next reaction.
3-(3-Iodo-phenyl)-benzo[d]isoxazole-6,7-diol (430 mg, 1.22 mmol), K2CO3 (379 mg, 2.75 mmol), 1,2-dibromoethane (210 μL), and ethylene glycol (2.05 mL) are heated at 120° C. for 6 h. The reaction mixture is diluted in H2O and is EtOAc-extracted. Purification by column (3:7 CH2Cl2:Hex) yields off-white solid product (209 mg, 45%).
3-(3-Iodo-phenyl-7,8-dihydro-1,6,9-trioxa-2-aza-cyclopenta[a]naphthalene (98 mg, 0.26 mmol) is suspended in THF (650 μL) at 0° C. under N2. Isopropylmagnesium chloride (195 μL, 2 M in THF, 0.39 mmol) is added dropwise. This is stirred at 0° C. for 30 min. CO2 gas is bubbled in for 10 minutes at 0° C., and for 45 min at rt (dry THF is added periodically to maintain solvent volume). The reaction mix is then quenched with aqueous HCl. This is EtOAc-extracted. The solid residue from the EtOAc layer is ether-triturated to yield product as a white solid (40 mg, 52%). 1H NMR (d-6 DMSO) σ: 4.4 (br s, 4H), 7.03 (d, 1H), 7.44 (d, 1H), 7.72 (t, 1H), 8.06-8.2 (m, 2H), 8.4 (s, 1H).
Similar compounds, such as Compound 134, may be prepared in a similar manner.
3-[1,3]Dioxolo[4′,5′:3,4]benzo[1,2-d]isoxazol-3-yl-benzoic acid (Compound 131) and similar compounds may generally be prepared according to Scheme G as follows.
3-(3-Iodo-phenyl)-benzo[d]isoxazole-6,7-diol (300 mg, 0.85 mmol), KF (450 mg, 7.75 mmol), DMF (2.3 mL), and dibromomethane (65 μL, 0.91 mmol). are heated at 140° C. for 4 h. The reaction mixture is diluted in H2O and is EtOAc-extracted. Purification by column (1:1 CH2Cl2:Hex) yields product as a white solid (166 mg, 54%).
3-(3-Iodo-phenyl)-[1,3]-dioxolo[4′,5′:3,4]benzo[1,2-d]isoxazole (97 mg, 0.27 mmol) is converted to white solid product (43 mg, 56%) by a procedure similar to Scheme F, step 5. 1H NMR (d-6 DMSO) σ: 6.28 (s, 2H), 7.23 (d, 1H), 7.58 (d, 1H), 7.76 (t, 1H), 8.08-8.22 (m, 2H), 8.41 (s, 1H).
Similar compounds, such as Compound 133, may be prepared in a similar manner.
4-(6-p-Tolyl-benzo[d]isoxazol-3-yl)-benzoic acid (Compound 138) and similar compounds of the invention may generally be prepared according to Scheme H as follows.
3-(4-Iodo-phenyl)-6-methoxy)-benzo[d]isoxazole (850 mg, 2.4 mmol) is prepared in a manner similar to Scheme E, step 3 to yield product as a tan solid (570 mg, 75%).
3-(4-Iodo-phenyl)-benzo[d]isoxazol-6-ol (337 mg, 1 mmol) is suspended in CH2Cl2 (1.6 mL) at 0° C. under N2. Pyridine (400 μL, 4.9 mmol) is added, followed by trifluoromethanesulfonic anhydride (210 μL, 1.25 mmol) dropwise. This is stirred at 0° C. for 30 min. The reaction mixture is then diluted with H2O, and the organic layer is separated. Purification by column (1:1 CH2Cl2:Hex) yields product as a clear oil (447 mg, 95%).
Trifluoro-methanesulfonic acid 3-(4-iodo-phenyl)-benzo[d]isoxazol-6-yl ester (390 mg, 0.83 mmol) is converted into white solid product (261 mg, 81%) at 85% purity using a procedure similar to Scheme F, step 5. The crude material is used as is in the next step.
4-(6-Trifluoromethylsulfonyloxy-benzo[d]isoxazol3-yl)-benzoic acid (41 mg, 0.1 mmol), p-tolylboronic acid (22 mg, 0.16 mmol), Pd(PPh3)4 (3.4 mg, 3 mole %), THF (1.2 mL), Na2CO3 (200 μL, 2 M in H2O), and a crystal of LiCl are heated at 60° C. for 5 h. The reaction mixture is aqueous HCl/EtOAc-extracted. The solid residue from the EtOAc layer is triturated with 3 mL acetone to yield solid white product (31 mg, 88%). 1H NMR (d-6 DMSO) σ: 2.38 (s, 3H), 7.30 (d, 2H), 7.66-7.78 (m, 3H), 8.05-8.20 (m, 6H).
Similar compounds, such as Compounds 135, 136, 137, 139, 140, 141, and 142, may be prepared in a similar manner.
Melting point and mass spec data for certain preferred compounds of the invention are presented in the table below.
A functional, cell-based translation assay based on luciferase-mediated chemoluminescence (International Application PCT/US2003/023185, filed on Jul. 23, 2003, hereby incorporated by reference in its entirety) permits quantitative assessment of the level of nonsense suppression. Human embryonic kidney cells (293 cells) are grown in medium containing fetal bovine serum (FBS). These cells can be stably transfected with the luciferase gene containing a premature termination codon at amino acid position 190. In place of the threonine codon (ACA) normally present in the luciferase gene at this site, each of the 3 possible nonsense codons (TAA, TAG, or TGA) and each of the 4 possible nucleotides (adenine, thymine, cytosine, or guanine) at the contextually important downstream +1 position following the nonsense codon are introduced by site-directed mutagenesis. As such, amino acid 190 in the luciferase gene containing a premature termination codon is TAA, TAG, or TGA. For each stop codon, the nucleotide following amino acid 190 of luciferase gene containing a premature termination codon can be replaced with an adenine, thymine, cytosine, or guanine (A, T, C, G) such that these mutations do not change the reading frame of the luciferase gene. Schematics of these constructs are depicted in
The nonsense suppression activity from a cell-based luciferase reporter assay of the present invention as described above shown in the table below (Table 2). Human Embryonic Kidney 293 cells are stably transfected with a luciferase reporter construct comprising a UGA nonsense mutation at position 190, which is followed, in-frame by an adenine nucleotide.
Activity measurements in Table 2 are determined in a cell-based luciferase reporter assay of the present invention construct containing a UGA premature termination codon. Gentamicin, an aminoglycoside antibiotic known to allow readthrough of premature termination codons, is used as an internal standard. Activity measurements are based on the qualitative ratio between the minimum concentration of compound required to produce a given protein in a cell versus the amount of protein produced by the cell at that concentration. Compounds which are found to have either or both very high potency and very high efficacy of protein synthesis are classified as “*****” Compounds which are found to have intermediate potency and/or efficacy of protein synthesis are classified as “****”; “***”; or “**”. Similarly, compounds which are found to have lower potency and/or efficacy of protein synthesis are classified as “*”.
A functional, cell-based translation assay based on luciferase-mediated chemoluminescence (International Application PCT/US2003/023185, filed on Jul. 23, 2003 and incorporated by reference in its entirety) permits assessment of translation-readthough of the normal stop codon in a mRNA. Human embryonic kidney cells (293 cells) are grown in medium containing fetal bovine serum (FBS). These cells are stably transfected with the luciferase gene containing a premature termination codon at amino acid position 190. In place of the threonine codon (ACA) normally present in the luciferase gene at this site, each of the 3 possible nonsense codons (TAA, TAG, or TGA) and each of the 4 possible nucleotides (adenine, thymine, cytosine, or guanine) at the contextually important downstream +1 position following the nonsense codon are introduced by site-directed mutagenesis. As such, amino acid 190 in the luciferase gene containing a premature termination codon is either TAA, TAG, or TGA. For each stop codon, the nucleotide following amino acid 190 of luciferase gene containing a premature termination codon are replaced with an adenine, thymine, cytosine, or guanine (A, T, C, G) such that these mutation do not change the reading frame of the luciferase gene. Schematics of these constructs are depicted above in
Another assay of the present invention can evaluate compounds that promote nonsense mutation suppression. The luciferase constructs described above in
Cells that harbor the constructs of
Compounds of the present invention selectively act on premature termination codons but not normal termination codons in mammals.
Rats and dogs are administered high doses of compound (up to 1800 mg/kg) by gavage (oral) once daily for 14 days. After the treatment, tissues are collected, lysates are prepared, and Western blot analysis is performed. Selection of the proteins for evaluation of normal termination codon readthrough is based primarily on the corresponding mRNA having a second stop codon in the 3′-UTR that is in-frame with the normal termination codon. Between these 2 stop codons, each selected protein has an intervening sequence of nucleotides that codes for an extension of the protein in the event of ribosomal readthrough of the first termination codon. If the compound has the capacity to induce nonspecific, ribosomal readthrough, an elongated protein is differentiated from the wild-type protein using Western blot. Tissues are collected from rats and are analyzed for suppression of the normal termination codon (UAA) in the vimentin mRNA. No evidence of suppression is apparent. Tissues are collected from dogs treated with compounds of the present invention. There is no evidence of suppression of the normal termination codon of beta actin, which harbors a UAG stop codon.
In healthy human volunteers, a single dose of a compound of the present invention (200 mg/kg) is administered orally. Blood samples are collected, plasma is prepared, and a Western blot is conducted using plasma samples from female and male subjects. C-reactive protein (CRP), which harbors a UGA termination codon, is used to determine if treatment of subjects with compounds of the present invention result in suppression of the normal termination codon in the CRP mRNA. A luciferase assay in combination with a premature termination assay demonstrates selective suppression of premature termination codons but not normal termination codons.
Animal model systems can also be used to demonstrate the safety and efficacy of a compound of the present invention. The compounds of the present invention are tested for biological activity using animal models for a disease, condition, or syndrome of interest. These include animals engineered to contain the target RNA element coupled to a functional readout system, such as a transgenic mouse.
Examples of animal models for cystic fibrosis include, but are not limited to, cftr(−/−) mice (see, e.g., Freedman et al., 2001, Gastroenterology 121(4):950-7), cftr(tm1HGU/tm1HGU) mice (see, e.g., Bernhard et al., 2001, Exp Lung Res 27(4):349-66), CFTR-deficient mice with defective cAMP-mediated Cl(−) conductance (see, e.g., Stotland et al., 2000, Pediatr Pulmonol 30(5):413-24), and C57BL/6-Cftr(m1UNC)/Cftr(m1UNC) knockout mice (see, e.g., Stotland et al., 2000, Pediatr Pulmonol 30(5):413-24).
Examples of animal models for muscular dystrophy include, but are not limited to, mouse, hamster, cat, dog, and C. elegans. Examples of mouse models for muscular dystrophy include, but are not limited to, the dy−/− mouse (see, e.g., Connolly et al., 2002, J Neuroimmunol 127(1-2):80-7), a muscular dystrophy with myositis (mdm) mouse mutation (see, e.g., Garvey et al., 2002, Genomics 79(2):146-9), the mdx mouse (see, e.g., Nakamura et al., 2001, Neuromuscul Disord 11(3):251-9), the utrophin-dystrophin knockout (dko) mouse (see, e.g., Nakamura et al., 2001, Neuromuscul Disord 11(3):251-9), the dy/dy mouse (see, e.g., Dubowitz et al., 2000, Neuromuscul Disord 10(4-5):292-8), the mdx(Cv3) mouse model (see, e.g., Pillers et al., 1999, Laryngoscope 109(8):1310-2), and the myotonic ADR-MDX mutant mice (see, e.g., Kramer et al., 1998, Neuromuscul Disord 8(8):542-50). Examples of hamster models for muscular dystrophy include, but are not limited to, sarcoglycan-deficient hamsters (see, e.g., Nakamura et al., 2001, Am J Physiol Cell Physiol 281(2):C690-9) and the BIO 14.6 dystrophic hamster (see, e.g., Schlenker & Burbach, 1991, J Appl Physiol 71(5):1655-62). An example of a feline model for muscular dystrophy includes, but is not limited to, the hypertrophic feline muscular dystrophy model (see, e.g., Gaschen & Burgunder, 2001, Acta Neuropathol (Berl) 101(6):591-600). Canine models for muscular dystrophy include, but are not limited to, golden retriever muscular dystrophy (see, e.g., Fletcher et al., 2001, Neuromuscul Disord 11(3):239-43) and canine X-linked muscular dystrophy (see, e.g., Valentine et al., 1992, Am J Med Genet. 42(3):352-6). Examples of C. elegans models for muscular dystrophy are described in Chamberlain & Benian, 2000, Curr Biol 10(21):R795-7 and Culette & Sattelle, 2000, Hum Mol Genet. 9(6):869-77.
Examples of animal models for familial hypercholesterolemia include, but are not limited to, mice lacking functional LDL receptor genes (see, e.g., Aji et al., 1997, Circulation 95(2):430-7), Yoshida rats (see, e.g., Fantappie et al., 1992, Life Sci 50(24):1913-24), the JCR:LA-cp rat (see, e.g., Richardson et al., 1998, Atherosclerosis 138(1):135-46), swine (see, e.g., Hasler-Rapacz et al., 1998, Am J Med Genet. 76(5):379-86), and the Watanabe heritable hyperlipidaemic rabbit (see, e.g., Tsutsumi et al., 2000, Arzneimittelforschung 50(2):118-21; Harsch et al., 1998, Br J Pharmacol 124(2):227-82; and Tanaka et al., 1995, Atherosclerosis 114(1):73-82).
An example of an animal model for human cancer, in general includes, but is not limited to, spontaneously occurring tumors of companion animals (see, e.g., Vail & MacEwen, 2000, Cancer Invest 18(8):781-92). Examples of animal models for lung cancer include, but are not limited to, lung cancer animal models described by Zhang & Roth (1994, In Vivo 8(5):755-69) and a transgenic mouse model with disrupted p53 function (see, e.g., Morris et al., 1998, J La State Med Soc 150(4):179-85). An example of an animal model for breast cancer includes, but is not limited to, a transgenic mouse that overexpresses cyclin D1 (see, e.g., Hosokawa et al., 2001, Transgenic Res 10(5):471-8). An example of an animal model for colon cancer includes, but is not limited to, a TCRbeta and p53 double knockout mouse (see, e.g., Kado et al., 2001, Cancer Res 61(6):2395-8). Examples of animal models for pancreatic cancer include, but are not limited to, a metastatic model of Panc02 murine pancreatic adenocarcinoma (see, e.g., Wang et al., 2001, Int J Pancreatol 29(1):37-46) and nu-nu mice generated in subcutaneous pancreatic tumours (see, e.g., Ghaneh et al., 2001, Gene Ther 8(3):199-208). Examples of animal models for non-Hodgkin's lymphoma include, but are not limited to, a severe combined immunodeficiency (“SCID”) mouse (see, e.g., Bryant et al., 2000, Lab Invest 80(4):553-73) and an IgHmu-HOX11 transgenic mouse (see, e.g., Hough et al., 1998, Proc Natl Acad Sci USA 95(23):13853-8). An example of an animal model for esophageal cancer includes, but is not limited to, a mouse transgenic for the human papillomavirus type 16 E7 oncogene (see, e.g., Herber et al., 1996, J Virol 70(3):1873-81). Examples of animal models for colorectal carcinomas include, but are not limited to, Apc mouse models (see, e.g., Fodde & Smits, 2001, Trends Mol Med 7(8):369-73 and Kuraguchi et al., 2000, Oncogene 19(50):5755-63). An example of an animal model for neurofibromatosis includes, but is not limited to, mutant NF1 mice (see, e.g., Cichowski et al., 1996, Semin Cancer Biol 7(5):291-8). Examples of animal models for retinoblastoma include, but are not limited to, transgenic mice that expression the simian virus 40 T antigen in the retina (see, e.g., Howes et al., 1994, Invest Opthalmol Vis Sci 35(2):342-51 and Windle et al, 1990, Nature 343(6259):665-9) and inbred rats (see, e.g., Nishida et al., 1981, Curr Eye Res 1(1):53-5 and Kobayashi et al., 1982, Acta Neuropathol (Berl) 57(2-3):203-8). Examples of animal models for Wilm's tumor include, but are not limited to, a WT1 knockout mice (see, e.g., Scharnhorst et al., 1997, Cell Growth Differ 8(2):133-43), a rat subline with a high incidence of neuphroblastoma (see, e.g., Mesfin & Breech, 1996, Lab Anim Sci 46(3):321-6), and a Wistar/Furth rat with Wilms' tumor (see, e.g., Murphy et al., 1987, Anticancer Res 7(4B):717-9).
Examples of animal models for retinitis pigmentosa include, but are not limited to, the Royal College of Surgeons (“RCS”) rat (see, e.g., Vollrath et al., 2001, Proc Natl Acad Sci USA 98(22);12584-9 and Hanitzsch et al., 1998, Acta Anat (Basel) 162(2-3):119-26), a rhodopsin knockout mouse (see, e.g., Jaissle et al., 2001, Invest Opthalmol Vis Sci 42(2):506-13), and Wag/Rij rats (see, e.g., Lai et al., 1980, Am J Pathol 98(1):281-4).
Examples of animal models for cirrhosis include, but are not limited to, CCl4-exposed rats (see, e.g., Kloehn et al., 2001, Horm Metab Res 33(7):394-401) and rodent models instigated by bacterial cell components or colitis (see, e.g., Vierling, 2001, Best Pract Res Clin Gastroenterol 15(4):591-610).
Examples of animal models for hemophilia include, but are not limited to, rodent models for hemophilia A (see, e.g., Reipert et al., 2000, Thromb Haemost 84(5):826-32; Jarvis et al.,. 1996, Thromb Haemost 75(2):318-25; and Bi et al., 1995, Nat Genet. 10(1):119-21), canine models for hemophilia A (see, e.g., Gallo-Penn et al., 1999, Hum Gene Ther 10(11):1791-802 and Connelly et al, 1998, Blood 91(9); 3273-81), murine models for hemophilia B (see, e.g., Snyder et al., 1999, Nat Med 5(1):64-70; Wang et al., 1997, Proc Natl Acad Sci USA 94(21):11563-6; and Fang et al., 1996, Gene Ther 3(3):217-22), canine models for hemophilia B (see, e.g., Mount et al., 2002, Blood 99(8):2670-6; Snyder et al., 1999, Nat Med 5(1):64-70; Fang et al., 1996, Gene Ther 3(3):217-22); and Kay et al., 1994, Proc Natl Acad Sci USA 91(6):2353-7), and a rhesus macaque model for hemophilia B (see, e.g., Lozier et al., 1999, Blood 93(6):1875-81).
Examples of animal models for von Willebrand disease include, but are not limited to, an inbred mouse strain RIIIS/J (see, e.g., Nichols et al., 1994, 83(11):3225-31 and Sweeney et al., 1990, 76(11):2258-65), rats injected with botrocetin (see, e.g., Sanders et al., 1988, Lab Invest 59(4):443-52), and porcine models for von Willebrand disease (see, e.g., Nichols et al., 1995, Proc Natl Acad Sci USA 92(7):2455-9; Johnson & Bowie, 1992, J Lab Clin Med 120(4):553-8); and Brinkhous et al., 1991, Mayo Clin Proc 66(7):733-42).
Examples of animal models for β-thalassemia include, but are not limited to, murine models with mutations in globin genes (see, e.g., Lewis et al., 1998, Blood 91(6):2152-6; Raja et al., 1994, Br J Haematol 86(1):156-62; Popp et al., 1985, 445:432-44; and Skow et al., 1983, Cell 34(3):1043-52).
Examples of animal models for kidney stones include, but are not limited to, genetic hypercalciuric rats (see, e.g., Bushinsky et al., 1999, Kidney Int 55(1):234-43 and Bushinsky et al., 1995, Kidney Int 48(6):1705-13), chemically treated rats (see, e.g., Grases et al., 1998, Scand J Urol Nephrol 32(4):261-5; Burgess et al., 1995, Urol Res 23(4):239-42; Kumar et al., 1991, J Urol 146(5):1384-9; Okada et al., 1985, Hinyokika Kiyo 31(4):565-77; and Bluestone et al., 1975, Lab Invest 33(3):273-9), hyperoxaluric rats (see, e.g., Jones et al., 1991, J Urol 145(4):868-74), pigs with unilateral retrograde flexible nephroscopy (see, e.g., Seifmah et al., 2001, 57(4):832-6), and rabbits with an obstructed upper urinary tract (see, e.g., Itatani et al., 1979, Invest Urol 17(3):234-40).
Examples of animal models for ataxia-telangiectasia include, but are not limited to, murine models of ataxia-telangiectasia (see, e.g., Barlow et al., 1999, Proc Natl Acad Sci USA 96(17):9915-9 and Inoue et al., 1986, Cancer Res 46(8):3979-82).
Examples of animal models for lysosomal storage diseases include, but are not limited to, mouse models for mucopolysaccharidosis type VII (see, e.g., Brooks et al., 2002, Proc Natl Acad Sci USA. 99(9):6216-21; Monroy et al., 2002, Bone 30(2):352-9; Vogler et al., 2001, Pediatr Dev Pathol. 4(5):421-33; Vogler et al., 2001, Pediatr Res. 49(3):342-8; and Wolfe et al., 2000, Mol. Ther. 2(6):552-6), a mouse model for metachromatic leukodystrophy (see, e.g., Matzner et al., 2002, Gene Ther. 9(1):53-63), a mouse model of Sandhoff disease (see, e.g., Sango et al., 2002, Neuropathol Appl Neurobiol. 28(1):23-34), mouse models for mucopolysaccharidosis type III A (see, e.g., Bhattacharyya et al., 2001, Glycobiology 11(1):99-10 and Bhaumik et al., 1999, Glycobiology 9(12):1389-96.), arylsulfatase A (ASA)-deficient mice (see, e.g., D'Hooge et al., 1999, Brain Res. 847(2):352-6 and D'Hooge et al, 1999, Neurosci Lett. 273(2):93-6); mice with an aspartylglucosaminuria mutation (see, e.g., Jalanko et al., 1998, Hum Mol. Genet. 7(2):265-72); feline models of mucopolysaccharidosis type VI (see, e.g., Crawley et al., 1998, J Clin Invest. 101(1):109-19 and Norrdin et al., 1995, Bone 17(5):485-9); a feline model of Niemann-Pick disease type C (see, e.g., March et al., 1997, Acta Neuropathol (Berl). 94(2):164-72); acid sphingomyelinase-deficient mice (see, e.g., Otterbach & Stoffel, 1995, Cell 81(7):1053-6), and bovine mannosidosis (see, e.g., Jolly et al., 1975, Birth Defects Orig Arctic Ser. 11(6):273-8).
Examples of animal models for tuberous sclerosis (“TSC”) include, but are not limited to, a mouse model of TSC1 (see, e.g., Kwiatkowski et al., 2002, Hum Mol. Genet. 11(5):525-34), a Tsc1 (TSC1 homologue) knockout mouse (see, e.g., Kobayashi et al., 2001, Proc Natl Acad Sci USA. 2001 Jul. 17; 98(15):8762-7), a TSC2 gene mutant(Eker) rat model (see, e.g., Hino 2000, Nippon Rinsho 58(6):1255-61; Mizuguchi et al., 2000, J Neuropathol Exp Neurol. 59(3):188-9; and Hino et al, 1999, Prog Exp Tumor Res. 35:95-108); and Tsc2(+/−) mice (see, e.g., Onda et al., 1999, J Clin Invest. 104(6):687-95).
The mutation in the mdx mouse that causes premature translation termination of the 427 kDa dystrophin polypeptide has been shown to be a C to T transition at position 3185 in exon 23 (Sicinski et al, Science 244(4912):1578-1580 (1989)). Mouse primary skeletal muscle cultures derived from 1-day old mdx mice are prepared as described previously (Barton-Davis et al., J. Clin. Invest. 104(4):375-381 (1999)). Cells are cultured for 10 days in the presence of a compound of the invention. Culture medium is replaced every four days and the presence of dystrophin in myoblast cultures is detected by immunostaining as described previously (Barton-Davis et al., J. Clin. Invest. 104(4):375-381 (1999)). A primary monoclonal antibody to the C-terminus of the dystrophin protein is used undiluted and rhodamine conjugated anti-mouse IgG is used as the secondary antibody. The antibody detects the full-length protein produced by suppression of the nonsense codon. Staining is viewed using a Leica DMR microscope, digital camera, and associated imaging software.
As previously described (Barton-Davis et al., J. Clin. Invest. 104(4):375-381(1999), compound is delivered by Alzet osmotic pumps implanted under the skin of anesthetized mice. Two doses of a compound of the invention are administered. Gentamicin serves as a positive control and pumps filled with solvent only serve as the negative control. Pumps are loaded with appropriate compound such that the calculated doses to which tissue is exposed are 10 mM and 20 mM. The gentamicin concentration is calculated to achieve tissue exposure of approximately 200 mM. In the initial experiment, mice are treated for 14 days, after which animals are anesthetized with ketamine and exsanguinated. The tibialis anterior (TA) muscle of the experimental animals is then excised, frozen, and used for immunofluorescence analysis of dystrophin incorporation into striated muscle. The presence of dystrophin in TA muscles is detected by immunostaining, as described previously (Barton-Davis et al., J. Clin. Invest. 104(4):375-381(1999).
Quadricep muscles from an mdx mouse treated with a compound of the present invention for 4 weeks are analyzed by western blot using a commercially available antibody to dystrophin. Protein extracted from the quadriceps of a wild-type mouse serve as a positive control. Production of full-length dystrophin is observed in the treated animal. The amount of full-length dystrophin produced, as a result of nonsense suppression, but not limited by this theory, is approximately 10% of wild-type levels of expression.
Male mdx mice (age 9-11 weeks) are treated with different compounds of the present invention (n=2 at least for each compound). These compounds are injected SQ once per day for two weeks at 25 mg/kg. After 2 weeks of treatment, mice are sacrificed for the removal of muscles to determine dystrophin readthrough efficiency.
Immunofluorescence (IF) is performed on 10 μm cryosections using a dystrophin antibody. The antibody recognizes an epitope C-terminal to the premature stop mutation found in mdx mice. Image analysis is performed in an identical manner in all sections. Images from treated and untreated mice are analyzed and a signal greater than the signal on the untreated control is deemed positive and indicates that suppression of the premature termination codon in the dystrophin mRNA occurred.
Isolated whole muscle mechanics is performed on EDL muscles from animals. Optimum muscle length (Lo) is defined as the length that produced maximum twitch tension. Maximum tetanic force at Lo is measured using a 120 Hz, 500 msec pulse at supramaximal voltage. Protection against mechanical injury, induced by a series of 5 eccentric tetanic contractions, is monitored. These measurements are performed using a 700 msec stimulation period during which the muscle is held in an isometric contraction for the first 500 msec followed by a stretch of 8 or 10% Lo at a rate of 0.5 Lo/sec. Protection against mechanical injury is evaluated at 80 Hz stimulation frequency. Damage is determined as the loss in force between the first and last eccentric contraction.
For an animal model system, CAOV-3 cells (1×107) are injected into the flanks of nude/nude mice. After 12 days, mice are randomized (10 mice per group) and treated subcutaneously (5 days per week) with 3 mg/kg of a compound of the present invention or intraperitonealy (1 day per week) with 30 mg/kg of a compound of the present invention. Tumor volumes are measured weekly. Suppression of nonsense mutations in the p53 gene by a compound of the present invention can inhibit cancer growth in vivo.
Previous studies have demonstrated that gentamicin and other members of the aminoglycoside family that decrease the fidelity of translation bind to the A site of the 16S rRNA. By chemical footprinting, UV cross-linking and NMR, gentamicin has been shown to bind at the A site (comprised of nucleotides 1400-1410 and 1490-1500, E. coli numbering) of the rRNA at nucleotides 1406, 1407, 1494, and 1496 (Moazed & Noller, Nature 327(6121):389-394 (1978); Woodcock et al., EMBO J. 10(10):3099-3103 (1991); and Schroeder et al., EMBO J. 19:1-9 (2000).
Ribosomes prepared from HeLa cells are incubated with the small molecules (at a concentration of 100 mM), followed by treatment with chemical modifying agents (dimethyl sulfate [DMS] and kethoxal [KE]). Following chemical modification, rRNA is phenol-chloroform extracted, ethanol precipitated, analyzed in primer extension reactions using end-labeled oligonucleotides hybridizing to different regions of the three rRNAs and resolved on 6% polyacrylamide gels. Probes for primer extension cover the entire 18S (7 oligonucleotide primers), 28S (24 oligonucleotide primers), and 5S (one primer) rRNAs. Controls in these experiments include DMSO (a control for changes in rRNA accessibility induced by DMSO), paromomycin (a marker for 18S rRNA binding), and anisomycin (a marker for 28S rRNA binding).
All publications and patent applications cited herein are incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference.
Although certain embodiments have been described in detail above, those having ordinary skill in the art will clearly understand that many modifications are possible in the embodiments without departing from the teachings thereof. All such modifications are intended to be encompassed within the claims of the invention.
This application claims priority to and the benefit under 35 U.S.C. §119 of U.S. Application Nos. 60/617,655, filed Oct. 13, 2004, 60/617,634, filed Oct. 13, 2004; 60/617,633, filed Oct. 13, 2004, 60/617,670, filed Oct. 13, 2004, all of which applications are herein incorporated by reference in their entireties. The present application also claims priority to and the benefit under 35 U.S.C. §119 of U.S. Application Nos. 60/617,653, filed Oct. 13, 2004, and 60/624,170, filed Nov. 3, 2004. U.S. Application No. 60/624,170, filed Nov. 3, 2004, is herein incorporated by reference in its entirety. The present application also incorporates by reference herein in their entireties International Patent Applications entitled “Compounds for Nonsense Suppression, and Methods for Their Use,” filed on Oct. 13, 2005 and identified as Attorney Docket Numbers 19025.040, 19025.041, 19025.042, and 19025.043.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US05/36762 | 10/13/2005 | WO | 00 | 6/13/2008 |
| Number | Date | Country | |
|---|---|---|---|
| 60617670 | Oct 2004 | US | |
| 60617633 | Oct 2004 | US | |
| 60617655 | Oct 2004 | US | |
| 60617634 | Oct 2004 | US | |
| 60617653 | Oct 2004 | US | |
| 60624170 | Nov 2004 | US |
