Patent Application
20180369210
The invention relates generally to the treatment of lysosomal storage disorders, and more specifically relates to the use of acid ceramidase inhibitors for the treatment of lysosomal storage disorders.
Lysosomal storage disorders (LSDs) are a group of more than 50 clinically-recognized, rare inherited metabolic disorders that result from defects in lysosomal function (Walkley, J. (2009) I
A deficiency of lysosomal enzyme activity can result in a massive accumulation in the lysosome of the substrate of the lysosomal enzyme at issue (Hers (1966) G
Individually, LSDs occur with incidences of less than 1:100,000, however, as a group the incidence is as high as 1 in 1,500 to 7,000 live births (Staretz-Chacham, et al. (2009) P
Typical treatment for many LSDs is enzyme replacement therapy (ERT) where the missing enzyme is given to the patient, usually through intravenous injection in large doses. This has been particularly useful in enzyme replacement therapy where an enzyme is administered to a subject to restore normal enzymatic function in the subject. By way of example, CEREZYME® (a recombinant β-glucocerebrosidase analogue) has been approved for the treatment of Type I Gaucher's Disease, VPRIV® (recombinant glucocerebrosidase, velaglucerase alfa) has been approved for the treatment of Gaucher's Disease Type I, FABRAZYME® (recombinant α-galactosidase) has been approved for the treatment of Fabry Disease, MYOZYME® (recombinant alglucosidase) has been approved for the treatment of Pompe Disease, LUMIZYME® (recombinant alglucosidase) has been approved for the treatment of late-onset Pompe Disease, and ELAPRASE® (recombinant iduronate-2-sulfatase) has been approved for the treatment of Hunter's Syndrome. Accordingly, enzyme replacement therapy for a variety of lysosomal storage diseases is being actively pursued.
ERT, however, only treats the symptoms of the disorder and is not curative, thus the patient must be given repeated injections of these proteins for the rest of their lives, and potentially may develop neutralizing antibodies to the injected protein. Often these proteins have a short serum half life, and so the patient must also receive frequent intravenous infusions of the protein. For example, Gaucher's disease patients receiving the CEREZYME® product must have infusions several times a week. Given their physical properties (including size and charge distribution), the active molecules in ERT usually are unable to traverse the blood-brain barrier, and as a result neurological symptoms of a given disorder may remain untreated. Furthermore, the production, purification, shipping, and storage of the enzymes can also problematic, and so the treatments can be very costly, with estimated costs being over $100,000 per year per patient.
Thus, there remains the need for additional methods and compositions for treating LSDs.
The invention is based, in part, upon the discovery that certain sphingosine-containing analogs accumulate to abnormal levels in the lysosomes of cells of subjects with LSDs, which can contribute to disease progression in those subjects. Given that acid ceramidase enzymes are involved in the conversion of ceramide-based substrates into sphingosine or sphingosine-containing analogs, acid ceramidase inhibitors can be used to treat LSDs, for example, to slow down, stop, or reverse the development of the LSD or ameliorate one or more symptoms of the LSD.
In one aspect, the invention provides a method of treating a LSD (e.g., Gaucher's disease, Krabbe disease, Fabry disease or Tay-Sachs disease) in a subject in need thereof. The method comprises administering to the subject an acid ceramidase inhibitor in an amount effective to treat the disorder in the subject. The acid ceramidase inhibitor can be administered to the subject so as to prevent the accumulation of sphingosine or a sphingosine-containing analog to a level found in subjects with the lysosomal disorder when compared to subjects without the disorder. In other words, the acid ceramidase prevents the accumulation of a target sphingosine or sphingosine-containing analog to a predetermined threshold concentration (for example, a median concentration determined by clinical analyses) found in subjects with the lysosomal storage disorder relative to subjects without the disorder (i.e., less than the predetermined threshold concentration).
It is contemplated that a variety of acid ceramidase inhibitors, either alone or in combination with other agents, may be useful in the treatment of the LSD. When administered, the acid ceramidase inhibitor prevents the accumulation of unwanted sphingosine or sphingosine-containing analogs, which are associated with the phenotype of the LSD. An exemplary acid ceramidase inhibitor useful in treating one or more of the LSDs described herein can be a compound of Formula I or Formula I-1 below, for example
or a pharmaceutically acceptable salt thereof, wherein:
A1 is a cyclic group selected from 5-6 membered heterocyclyl, 5-6 membered heteroaryl, and bicyclic heterocyclyl, each of which is substituted by 1, 2, 3, or 4 occurrences of R2;
R1 represents independently for each occurrence hydrogen, C1-4alkyl, —C1-4alkyl-phenyl, —CO2—C1-6alkyl, —C(O)—NH2, —C(O)—NH—C1-6alkyl, or —C(O)—N(C1-6alkyl)2;
R2 represents independently for each occurrence R1, C1-4alkyl, C1-4haloalkyl, C1-4 alkoxy, halogen, hydroxyl, oxo, cyano, nitro, azido, —N(R1)2, —C(O)—C1-4alkyl, —C(O)-phenyl, —CO2—R1, —C(O)—NH2, —C(O)—NH—C1-6alkyl, —C(O)—N(C1-4alkyl)2, —O—C(O)—NH2, —O—C(O)—NH—C1-6alkyl, —O—C(O)—N(C1-6alkyl)2, —C1-4alkyl-phenyl, C3-10cycloalkyl, C3-10heterocyclyl, 6-10 membered aryl, 6-10 membered heteroaryl, —C1-4alkylene-C3-10cycloalkyl, —C1-4alkylene-C3-10heterocyclyl, —(C1-4alkylene)-6-10 membered aryl, or —(C1-4alkylene)-6-10 membered heteroaryl;
Y1 represents:
W1 represents:
or a pharmaceutically acceptable salt thereof, wherein:
A1 is a cyclic group selected from 5-6 membered heterocyclyl, 5-6 membered heteroaryl, and bicyclic heterocyclyl, each of which is substituted by 1, 2, or 3 occurrences of R2;
R1 represents independently for each occurrence hydrogen, C1-4alkyl, —C1-4alkyl-phenyl, —CO2—C1-4alkyl, —C(O)—NH2, —C(O)—NH—C1-6alkyl, or —C(O)—N(C1-6alkyl)2;
R2 represents independently for each occurrence R1, C1-4alkyl, C1-4haloalkyl, C1-4alkoxy, halogen, hydroxyl, oxo, cyano, nitro, azido, —N(R1)2, —C(O)—C1-4alkyl, —C(O)-phenyl, —CO2—R1, —C(O)—NH2, —C(O)—NH—C1-6alkyl, —C(O)—N(C1-6alkyl)2, —O—C(O)—NH2, —O—C(O)—NH—C1-6alkyl, —O—C(O)—N(C1-6alkyl)2, —C1-4alkyl-phenyl, C3-10cycloalkyl, C3-10heterocyclyl, 6-10 membered aryl, 6-10 membered heteroaryl, —C1-4alkylene-C3-10cycloalkyl, —C1-4alkylene-C3-10 heterocyclyl, —C1-4alkylene-6-10 membered aryl, or —C1-4alkylene-6-10 membered heteroaryl;
Y1 represents:
In certain embodiments, the acid ceramidase inhibitor is selected from the group consisting of:
pharmaceutically acceptable salts thereof.
In certain embodiments, the acid ceramidase inhibitor is a uracil analog, for example, a 5-fluorouracil analog. In one embodiment, the acid ceramidase inhibitor is 1-hexylcarbamoyl-5-fluorouracil, also known as Carmofur, whose chemical structure shown below:
It is contemplated that, when the acid ceramidase inhibitor is a 5-fluorouracil analog, such as Carmofur, the 5-fluorouracil analog is administered at a concentration sufficient to inhibit acid ceramidase without substantially inhibiting thymidylate synthase.
In certain embodiments, the acid ceramidase inhibitor is administered at a concentration in the range from 0.01-200 mg/kg (for example, less than 20 mg/kg). In certain other embodiments, the acid ceramidase inhibitor is administered to a subject in the range from 0.01-200 mg/kg and at a dose sufficient to inhibit or reduce acid ceramidase activity but without substantially inhibiting (e.g., inhibiting less than 50%, 40%, 30%, 20%, 10%, or 5%) thymidylate synthase activity as determined in a cell or tissue sample using in vitro assays for measuring acid ceramidase activity, for example, as described in Bedia et al. (2010) J. L
The acid ceramidase inhibitors can be administered either alone or in combination with other agents for treating the LSD. For example, the acid ceramidase inhibitor can be administered to a subject that is undergoing or will be treated with (i) a recombinant enzyme as an ERT to supplement to the defective enzyme in the subject, (ii) an enzyme activator, for example, a glucocerebrosidase activator in the case of deficient glucocerebrosidase activity in subjects with Gaucher's disease, or (ii) a combination or (i) and (ii). In such an approach, the acid ceramidase inhibitor prevents the accumulation of sphingosine or sphingosine-containing analogs to a toxic or otherwise detrimental level in the lysosomal compartment of cells in the subject while increasing or supplementing the activity of the defective enzyme in the lysosomal compartment of cells in the subject.
These and other aspects and embodiments will be apparent from the following figures, detailed description, and claims.
The invention is based, in part, upon the discovery that sphingosine-containing analogs (for example, glucosylsphingosine, galactosphingosine, lactosylsphingosine, GB3-sphingosine, and GM2-sphingosine) may accumulate in cells of subjects with certain LSDs (for example, Gauchers disease, Krabbe disease, multiple sclerosis, Fabry's disease, and Tay Sachs disease, respectively) and that the accumulation of these sphingosine-containing analogs may contribute to the disease phenotype. Given that these sphingosine-containing analogs are produced by acid ceramidase enzymes in the lysosomal compartments of cells in subjects with LSDs, the accumulation of the sphingosine-containing analogs to detrimental levels can be prevented by the use of an effective amount of one or more inhibitors of acid ceramidase activity.
Although defective enzyme activity (for example, &f-glucocerebrosidase activity, as implicated in Gaucher's disease) may result in an accumulation of the substrate for that enzyme (for example, glucosylceramide) it has been observed that the accumulation of these substrates may also result in an accumulation of certain sphingosine-containing analogs (for example, glucosylsphingosine), whose accumulation may also be involved with the disease phenotype. The sphingosine-containing analogs are derived from the accumulated ceramide-based substrates by reactions catalyzed by an acid ceramidase.
In Gaucher's disease, for example, glucosylceramide (GlcCer) that accumulates as a result of deficient β-glucocerebrosidase activity can be converted into glucosylsphingosine (GluSph) via an acid ceramidase enzyme (a glycosylceramide to glycosylsphingosine converting enzyme). As a result, the accumulation of glucosylceramide (caused by defective β-glucocerebrosidase) may result in an accumulation of glucosylsphingosine, which is involved in disease progression in subjects with Gaucher's disease. Given that the conversion of glucosylceramide to glucosphingosine is catalyzed by an acid ceramidase enzyme, the administration of an acid ceramidase inhibitor can prevent the accumulation of glucosphingosine to a concentration or level within lysosomal compartment of cells that is toxic or otherwise detrimental to the cells. As a result, administration of an acid ceramidase inhibitor can reduce the accumulation of glucosphingosine thereby treating Gaucher's disease, which includes ameliorating a symptom associated with Gaucher's disease.
Similarly, in the case of Fabry's disease, defective α-galactoside A results in the accumulation of globotriaosylceramide (Gb3), which in turn can be converted into Gb3-sphingosine via an acid ceramidase (a globotriaosylceramide to Gb3-sphingosine converting enzyme). Given the accumulation of Gb3-sphingosine to a concentration or level in the lysosomal compartments of cells that is toxic or otherwise detrimental to the cells in subjects with Fabry's disease, the administration of an acid ceramidase inhibitor can reduce the accumulation of Gb3-sphingosine thereby treating Fabry's disease, which includes ameliorating a symptom associated with Fabry's disease.
Similarly, in case of Krabbe's disease, defective β-galactosyl-ceramidase results in the accumulation of galactoceramide (GalCer), which in turn can be converted into galactosphingosine (GalSph) via an acid ceramidase (a galactoceramide to galactosphingosine converting enzyme). Given the accumulation of galactoceramide to a concentration or level in the lysosomal compartments of cells that is toxic or otherwise detrimental to the cells in subjects with Krabbe's disease, the administration of an acid ceramidase inhibitor can reduce the accumulation of galactosphingosine thereby treating Krabbe's disease, which includes ameliorating a symptom associated with Krabbe's disease.
In addition, in the case of Tay-Sachs disease (or also Sandhoff Variant A, B), defective β-hexosaminidase results in the accumulation of monosialtrihexosylganglioside (GM2), which in turn can be converted into GM2-sphingosine via an acid ceramidase (a GM2 to GM2-sphingosine converting enzyme). Given the accumulation of the GM2-sphingosine to a concentration or level in the lysosomal compartments of cells that is toxic or otherwise detrimental to the cells in subjects with Tay-Sachs disease, the administration of an acid ceramidase inhibitor can reduce the accumulation of GM2-sphingosine thereby treating Tay-Sachs disease (or also Sandhoff Variant AB), which includes ameliorating a symptom associated with Tay-Sachs disease (or also Sandhoff Variant AB).
In the case of Niemann-Pick types A and B, defective sphingomyelinase results in the accumulation of sphingomyelin, which in turn can be converted into lyso-sphingomyelin via an acid ceramidase (a sphingomyelin to lyso-sphingomyelin converting enzyme). Given the accumulation of lyso-sphingomyelin to a concentration or level in the lysosomal compartments of cells that is toxic or otherwise detrimental to the cells in subjects with Niemann-Pick Type A, B, the administration of an acid ceramidase inhibitor can reduce the accumulation of lyso-sphingomyelin thereby treating Niemann-Pick type A and B, which includes ameliorating a symptom associated with Niemann-Pick type A and B.
To facilitate an understanding of the present invention, a number of terms and phrases are defined below.
The terms “a” and “an” as used herein mean “one or more” and include the plural unless the context is inappropriate.
The term “acid ceramidase” is understood to mean an amidase enzyme that catalyzes the conversion of ceramide or ceramide-based substrates to their respective sphingosine or sphingosine-containing analogs via a deacylation reaction.
The term “acid ceramidase inhibitor” is understood to mean a compound that preferentially reduces the activity of an acid ceramidase enzyme relative to other mammalian enzymes, for example, other enzymes present in lysosomes of mammalian cells.
A “lysosomal storage disorder or LSD” is understood to mean a disorder associated with a deficiency in a glycosphingolipid hydrolase activity (either by a complete or partial loss of activity) in the lysosomes of mammalian cells. As a result of the deficiency of the glycosphingolipid hydrolase activity, the cells accumulate the substrate of the particular hydrolase. Exemplary, lysosomal storage disorders include, Gaucher's disease, Krabbe's disease, Fabry's disease, Tay-Sachs disease, Sandhoff Variant AB disease, Niemann-Pick types A and B.
The term “alkyl” as used herein refers to a saturated straight or branched hydrocarbon, such as a straight or branched group of 1-12, 1-10, or 1-6 carbon atoms, referred to herein as C1-C12alkyl, C1-C10alkyl, and C1-C6alkyl, respectively. Exemplary alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, 2-methyl-1-propyl, 2-methyl-2-propyl, 2-methyl-1-butyl, 3-methyl-1-butyl, 2-methyl-3-butyl, 2,2-dimethyl-1-propyl, 2-methyl-1-pentyl, 3-methyl-1-pentyl, 4-methyl-1-pentyl, 2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl, 2,2-dimethyl-1-butyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, butyl, isobutyl, t-butyl, pentyl, isopentyl, neopentyl, hexyl, heptyl, octyl, etc.
The term “alkylene” refers to a diradical of an alkyl group. An exemplary alkylene group is —CH2CH2—.
The term “haloalkyl” refers to an alkyl group that is substituted with at least one halogen. For example, —CH2F, —CHF2, —CF3, —CH2CF3, —CF2CF3, and the like.
The term “heteroalkyl” as used herein refers to an “alkyl” group in which at least one carbon atom has been replaced with a heteroatom (e.g., an O, N, or S atom). The heteroalkyl may be, for example, an —O—C1-C10alkyl group, an —C1-C6alkylene-O—C1-C6alkyl group, or a C1-C6 alkylene-OH group. In certain embodiments, the “heteroalkyl” may be 2-8 membered heteroalkyl, indicating that the heteroalkyl contains from 2 to 8 atoms selected from the group consisting of carbon, oxygen, nitrogen, and sulfur. In yet other embodiments, the heteroalkyl may be a 2-6 membered, 4-8 membered, or a 5-8 membered heteroalkyl group (which may contain for example 1 or 2 heteroatoms selected from the group oxygen and nitrogen). One type of heteroalkyl group is an “alkoxyl” group.
The term “alkenyl” as used herein refers to an unsaturated straight or branched hydrocarbon having at least one carbon-carbon double bond, such as a straight or branched group of 2-12, 2-10, or 2-6 carbon atoms, referred to herein as C2-C12alkenyl, C2-C10alkenyl, and C2-C6alkenyl, respectively. Exemplary alkenyl groups include vinyl, allyl, butenyl, pentenyl, hexenyl, butadienyl, pentadienyl, hexadienyl, 2-ethylhexenyl, 2-propyl-2-butenyl, 4-(2-methyl-3-butene)-pentenyl, and the like.
The term “alkynyl” as used herein refers to an unsaturated straight or branched hydrocarbon having at least one carbon-carbon triple bond, such as a straight or branched group of 2-12, 2-10, or 2-6 carbon atoms, referred to herein as C2-C12alkynyl, C2-C10alkynyl, and C2-C6alkynyl, respectively. Exemplary alkynyl groups include ethynyl, prop-1-yn-1-yl, and but-1-yn-1-yl.
The term “cycloalkyl” refers to a monovalent cyclic, bicyclic, or bridged cyclic (e.g., adamantyl) hydrocarbon group of 3-12, 3-8, 4-8, or 4-6 carbons, referred to herein, e.g., as “C4-8cycloalkyl.” Cycloalkyl may contain one or more double bonds but does not have a completely conjugated pi-electron system. Exemplary cycloalkyl groups include, but are not limited to, cyclohexanes, cyclopentanes, cyclobutanes and cyclopropanes. Unless specified otherwise, cycloalkyl groups are optionally substituted at one or more ring positions with, for example, alkanoyl, alkoxy, alkyl, haloalkyl, alkenyl, alkynyl, amido, amidino, amino, aryl, arylalkyl, nitro, azido, carbamate, carbonate, carboxy, cyano, cycloalkyl, ester, ether, formyl, halogen, haloalkyl, heteroaryl, heterocyclyl, hydroxyl, imino, ketone, nitro, phosphate, phosphonato, phosphinato, sulfate, sulfide, sulfonamido, sulfonyl or thiocarbonyl. Cycloalkyl groups can be fused to other cycloalkyl, aryl, or heterocyclyl groups. In certain embodiments, the cycloalkyl group is not substituted, i.e., it is unsubstituted.
The term “cycloalkylene” refers to a diradical of an cycloalkyl group. An exemplary cycloalkylene group is
The term “cycloalkenyl” as used herein refers to a monovalent unsaturated cyclic, bicyclic, or bridged cyclic (e.g., adamantyl) hydrocarbon group of 3-12, 3-8, 4-8, or 4-6 carbons containing one carbon-carbon double bond, referred to herein, e.g., as “C4-8 cycloalkenyl,” derived from a cycloalkane. Exemplary cycloalkenyl groups include, but are not limited to, cyclohexenes, cyclopentenes, and cyclobutenes. Unless specified otherwise, cycloalkenyl groups are optionally substituted at one or more ring positions with, for example, alkanoyl, alkoxy, alkyl, alkenyl, alkynyl, amido, amidino, amino, aryl, arylalkyl, nitro, azido, carbamate, carbonate, carboxy, cyano, cycloalkyl, ester, ether, formyl, halogen, haloalkyl, heteroaryl, heterocyclyl, hydroxyl, imino, ketone, nitro, phosphate, phosphonato, phosphinato, sulfate, sulfide, sulfonamido, sulfonyl or thiocarbonyl. In certain embodiments, the cycloalkenyl group is not substituted, i.e., it is unsubstituted.
The term “aryl” is art-recognized and refers to a carbocyclic aromatic group. Representative aryl groups include phenyl, naphthyl, anthracenyl, and the like. The term “aryl” includes polycyclic ring systems having two or more carbocyclic rings in which two or more carbons are common to two adjoining rings (the rings are “fused rings”) wherein at least one of the rings is aromatic and, e.g., the other ring(s) may be cycloalkyls, cycloalkenyls, cycloalkynyls, and/or aryls. Unless specified otherwise, the aromatic ring may be substituted at one or more ring positions with, for example, halogen, nitro, azide, alkyl, aralkyl, alkenyl, alkynyl, cycloalkyl, hydroxyl, alkoxyl, amino, nitro, sulfhydryl, imino, amido, carboxylic acid, —C(O)alkyl, —CO2alkyl, carbonyl, carboxyl, alkylthio, sulfonyl, sulfonamido, sulfonamide, ketone, aldehyde, ester, heterocyclyl, aryl or heteroaryl moieties, —CF3, —CN, or the like. In certain embodiments, the aromatic ring is substituted at one or more ring positions with halogen, alkyl, hydroxyl, or alkoxyl. In certain other embodiments, the aromatic ring is not substituted, i.e., it is unsubstituted. In certain embodiments, the aryl group is a 6-10 membered ring structure.
The term “aralkyl” refers to an alkyl group substituted with an aryl group.
The term “bicyclic carbocyclyl that is partially unsaturated” refers to a bicyclic carbocyclic group containing at least one double bond between ring atoms and at least one ring in the bicyclic carbocyclic group is not aromatic. Representative examples of a bicyclic carbocyclyl that is partially unsaturated include, for example:
The terms ortho, meta and para are art-recognized and refer to 1,2-, 1,3- and 1,4-disubstituted benzenes, respectively. For example, the names 1,2-dimethylbenzene and ortho-dimethylbenzene are synonymous.
The terms “heterocyclyl” and “heterocyclic group” are art-recognized and refer to saturated, partially unsaturated, or aromatic 3- to 10-membered ring structures, alternatively 3- to 7-membered rings, whose ring structures include one to four heteroatoms, such as nitrogen, oxygen, and sulfur. The number of ring atoms in the heterocyclyl group can be specified using Cx-Cx nomenclature where x is an integer specifying the number of ring atoms. For example, a C3-C7heterocyclyl group refers to a saturated or partially unsaturated 3- to 7-membered ring structure containing one to four heteroatoms, such as nitrogen, oxygen, and sulfur. The designation “C3-C7” indicates that the heterocyclic ring contains a total of from 3 to 7 ring atoms, inclusive of any heteroatoms that occupy a ring atom position. One example of a C3heterocyclyl is aziridinyl. Heterocycles may also be mono-, bi-, or other multi-cyclic ring systems. A heterocycle may be fused to one or more aryl, partially unsaturated, or saturated rings. Heterocyclyl groups include, for example, biotinyl, chromenyl, dihydrofuryl, dihydroindolyl, dihydropyranyl, dihydrothienyl, dithiazolyl, homopiperidinyl, imidazolidinyl, isoquinolyl, isothiazolidinyl, isooxazolidinyl, morpholinyl, oxolanyl, oxazolidinyl, phenoxanthenyl, piperazinyl, piperidinyl, pyranyl, pyrazolidinyl, pyrazolinyl, pyridyl (i.e., pyridinyl), pyrimidinyl, pyrrolidinyl, pyrrolidin-2-onyl, pyrrolinyl, tetrahydrofuryl, tetrahydroisoquinolyl, tetrahydropyranyl, tetrahydroquinolyl, thiazolidinyl, thiolanyl, thiomorpholinyl, thiopyranyl, xanthenyl, lactones, lactams such as azetidinones and pyrrolidinones, sultams, sultones, and the like. Heterocyclyl groups also include, for example, furanyl, pyrrolyl, thiophenyl, pyrazolyl, oxazolyl, thiazolyl, tetrahydropyrimidinyl, pyrazinyl, dihydroisooxazolyl, isooxazolyl, isothiazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, imidazolinyl, imidazolidinyl, oxazolinyl, pyrazolinyl, thiazolinyl, triazolinyl, dihydrobenzooxazolyl, dihydrobenzoisoxazole, dihydrobenzothiazolyl, dihydrooxazolopyridinyl, dihydroimidazopyridinyl, dihydropyrazolopyridinyl, dihydroindazolyl, dihydrobenzoisothiazolyl, dihydroisothiazolopyridine, indazolyl, benzotriazolyl, triazolopyridine, and the like. Unless specified otherwise, the heterocyclic ring is optionally substituted at one or more positions with substituents such as alkanoyl, alkoxy, alkyl, alkenyl, alkynyl, amido, amidino, amino, aryl, arylalkyl, nitro, azido, carbamate, carbonate, carboxy, cyano, cycloalkyl, ester, ether, formyl, halogen, haloalkyl, heteroaryl, heterocyclyl, hydroxyl, imino, ketone, nitro, oxo, phosphate, phosphonato, phosphinato, sulfate, sulfide, sulfonamido, sulfonyl and thiocarbonyl. In certain embodiments, the heterocyclyl group is not substituted, i.e., it is unsubstituted.
The term “bicyclic heterocyclyl” refers to a heterocyclyl group that contains two rings that are fused together. Representative examples of a bicyclic heterocyclyl include, for example:
In certain embodiments, the bicyclic heterocyclyl is an carbocyclic ring fused to partially unsaturated heterocyclic ring, that together form a bicyclic ring structure having 8-10 ring atoms (e.g., where there are 1, 2, 3, or 4 heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur).
The term “heterocycloalkyl” is art-recognized and refers to a saturated heterocyclyl group as defined above. In certain embodiments, the “heterocycloalkyl” is a 3- to 10-membered ring structures, alternatively a 3- to 7-membered rings, whose ring structures include one to four heteroatoms, such as nitrogen, oxygen, and sulfur.
The term “heterocycloalkylene” refers to a diradical of a heterocycloalkyl group. An exemplary heterocycloalkylene group is
The heterocycloalkylene may contain, for example, 3-6 ring atom (i.e., a 3-6 membered heterocycloalkylene). In certain embodiments, the heterocycloalkylene is a 3-6 membered heterocycloalkylene containing 1, 2, or 3 three heteroatoms selected from the group consisting of oxygen, nitrogen, and sulfur.
The term “heteroaryl” is art-recognized and refers to aromatic groups that include at least one ring heteroatom. In certain instances, a heteroaryl group contains 1, 2, 3, or 4 ring heteroatoms. Representative examples of heteroaryl groups include pyrrolyl, furanyl, thiophenyl, imidazolyl, oxazolyl, thiazolyl, triazolyl, pyrazolyl, pyridinyl, pyrazinyl, pyridazinyl and pyrimidinyl, and the like. Unless specified otherwise, the heteroaryl ring may be substituted at one or more ring positions with, for example, halogen, azide, alkyl, aralkyl, alkenyl, alkynyl, cycloalkyl, hydroxyl, alkoxyl, amino, nitro, sulfhydryl, imino, amido, carboxylic acid, —C(O)alkyl, —CO2alkyl, carbonyl, carboxyl, alkylthio, sulfonyl, sulfonamido, sulfonamide, ketone, aldehyde, ester, heterocyclyl, aryl or heteroaryl moieties, —CF3, —CN, or the like. The term “heteroaryl” also includes polycyclic ring systems having two or more rings in which two or more carbons are common to two adjoining rings (the rings are “fused rings”) wherein at least one of the rings is heteroaromatic, e.g., the other cyclic rings may be cycloalkyls, cycloalkenyls, cycloalkynyls, and/or aryls. In certain embodiments, the heteroaryl ring is substituted at one or more ring positions with halogen, alkyl, hydroxyl, or alkoxyl. In certain other embodiments, the heteroaryl ring is not substituted, i.e., it is unsubstituted. In certain embodiments, the heteroaryl group is a 5- to 10-membered ring structure, alternatively a 5- to 6-membered ring structure, whose ring structure includes 1, 2, 3, or 4 heteroatoms, such as nitrogen, oxygen, and sulfur.
The term “heteroaralkyl” refers to an alkyl group substituted with a heteroaryl group.
The terms “amine” and “amino” are art-recognized and refer to both unsubstituted and substituted amines, e.g., a moiety represented by the general formula —N(R50)(R51), wherein R50 and R51 each independently represent hydrogen, alkyl, cycloalkyl, heterocyclyl, alkenyl, aryl, aralkyl, or —(CH2)m—R61; or R50 and R51, taken together with the N atom to which they are attached complete a heterocycle having from 4 to 8 atoms in the ring structure; R61 represents an aryl, a cycloalkyl, a cycloalkenyl, a heterocycle or a polycycle; and m is zero or an integer in the range of 1 to 8. In certain embodiments, R50 and R51 each independently represent hydrogen, alkyl, alkenyl, or —(CH2)m—R61.
The terms “alkoxyl” or “alkoxy” are art-recognized and refer to an alkyl group, as defined above, having an oxygen radical attached thereto. Representative alkoxyl groups include methoxy, ethoxy, propyloxy, tert-butoxy and the like. An “ether” is two hydrocarbons covalently linked by an oxygen. Accordingly, the substituent of an alkyl that renders that alkyl an ether is or resembles an alkoxyl, such as may be represented by one of —O-alkyl, —O— alkenyl, —O-alkynyl, —O—(CH2)m—R61, where m and R61 are described above.
The term “carbamate” as used herein refers to a radical of the form —RgOC(O)N(Rh)—, —RgOC(O)N(Rh)Ri—, or —OC(O)NRhRi, wherein Rg, Rh and Ri are each independently alkoxy, aryloxy, alkyl, alkenyl, alkynyl, amide, amino, aryl, arylalkyl, carboxy, cyano, cycloalkyl, ester, ether, formyl, halogen, haloalkyl, heteroaryl, heterocyclyl, hydroxyl, ketone, nitro, sulfide, sulfonyl, or sulfonamide. Exemplary carbamates include arylcarbamates and heteroaryl carbamates, e.g., wherein at least one of Rg, Rh and Ri are independently aryl or heteroaryl, such as phenyl and pyridinyl.
The term “carbonyl” as used herein refers to the radical —C(O)—.
The term “carboxamido” as used herein refers to the radical —C(O)NRR′, where R and R′ may be the same or different. R and R′ may be independently alkyl, aryl, arylalkyl, cycloalkyl, formyl, haloalkyl, heteroaryl, or heterocyclyl.
The term “carboxy” as used herein refers to the radical —COOH or its corresponding salts, e.g. —COONa, etc.
The term “amide” or “amido” as used herein refers to a radical of the form —RaC(O)N(Rb)—, —RaC(O)N(Rb)Rc—, —C(O)NRbRc, or —C(O)NH2, wherein Ra, Rb and Rc are each independently alkoxy, alkyl, alkenyl, alkynyl, amide, amino, aryl, arylalkyl, carbamate, cycloalkyl, ester, ether, formyl, halogen, haloalkyl, heteroaryl, heterocyclyl, hydrogen, hydroxyl, ketone, or nitro. The amide can be attached to another group through the carbon, the nitrogen, Rb, Rc, or Ra. The amide also may be cyclic, for example Rb and Rb, Ra and Rb, or Ra and Rb may be joined to form a 3- to 12-membered ring, such as a 3- to 10-membered ring or a 5- to 6-membered ring.
The term “amidino” as used herein refers to a radical of the form —C(═NR)NR′R″ where R, R′, and R″ are each independently alkyl, alkenyl, alkynyl, amide, aryl, arylalkyl, cyano, cycloalkyl, haloalkyl, heteroaryl, heterocyclyl, hydroxyl, ketone, or nitro.
The term “alkanoyl” as used herein refers to a radical —O—CO-alkyl.
The term “oxo” is art-recognized and refers to a “═O” substituent. For example, a cyclopentane substituted with an oxo group is cyclopentanone.
The term “sulfonamide” or “sulfonamido” as used herein refers to a radical having the structure —N(Rr)—S(O)2—Rs— or —S(O)2—N(Rr)Rs, where Rr, and Rs can be, for example, hydrogen, alkyl, aryl, cycloalkyl, and heterocyclyl. Exemplary sulfonamides include alkylsulfonamides (e.g., where Rs is alkyl), arylsulfonamides (e.g., where Rs is aryl), cycloalkyl sulfonamides (e.g., where Rs is cycloalkyl), and heterocyclyl sulfonamides (e.g., where Rs is heterocyclyl), etc.
The term “sulfonyl” as used herein refers to a radical having the structure RuSO2—, where Ru can be alkyl, aryl, cycloalkyl, and heterocyclyl, e.g., alkylsulfonyl. The term “alkylsulfonyl” as used herein refers to an alkyl group attached to a sulfonyl group.
The symbol “” indicates a point of attachment.
Unless otherwise indicated, the term “substituted” as used herein means that one or more hydrogen atoms of the above mentioned groups are replaced with another atom or functional group including, by way of example, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, alkoxy, cycloalkyloxy, aryloxy, arylalkyloxy, hydroxy, heteroaryl, heteroaryloxy, heterocyclyloxy, trifluoromethyl, trifluoromethoxy, carboxy, acyl, aroyl, heteroaroyl, halogen, nitro, cyano, alkoxycarbonyl, aryloxycarbonyl, aralkyloxycarbonyl, cycloalkyloxycarbonyl, heteroaryloxycarbonyl, acyloxy, alkylthio, arylthio, alkysulfinyl, arylsulfinyl, alkylsulfonyl, arylsulfonyl, —O-aroyl, —O-heteroaroyl, oxo (═O), —C(═O)—NRhRk, and —NRpRq, wherein each of Rh, Rk, Rp, and Rq independently represents hydrogen, unsubstituted or substituted alkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted aryl, unsubstituted or substituted arylalkyl, unsubstituted or substituted heteroaryl, unsubstituted or substituted heterocyclyl, acyl, aroyl, heteroaroyl, and when Rh and Rk, or Rp and Rq are taken together with the nitrogen atom to which they are bound, the group —NRhRk or the group NRpRq represent a heterocyclyl residue and wherein the terms alkyl, cycloalkyl, aryl, heteroaryl, heterocyclyl are as defined herein.
The compounds of the disclosure may contain one or more chiral centers and/or double bonds and, therefore, exist as stereoisomers, such as geometric isomers, enantiomers or diastereomers. The term “stereoisomers” when used herein consist of all geometric isomers, enantiomers or diastereomers. These compounds may be designated by the symbols “R” or “S,” depending on the configuration of substituents around the stereogenic carbon atom. The present invention encompasses various stereoisomers of these compounds and mixtures thereof. Stereoisomers include enantiomers and diastereomers. Mixtures of enantiomers or diastereomers may be designated “(±)” in nomenclature, but the skilled artisan will recognize that a structure may denote a chiral center implicitly. It is understood that graphical depictions of chemical structures, e.g., generic chemical structures, encompass all stereoisomeric forms of the specified compounds, unless indicated otherwise.
Individual stereoisomers of compounds of the present invention can be prepared synthetically from commercially available starting materials that contain asymmetric or stereogenic centers, or by preparation of racemic mixtures followed by resolution methods well known to those of ordinary skill in the art. These methods of resolution are exemplified by (1) attachment of a mixture of enantiomers to a chiral auxiliary, separation of the resulting mixture of diastereomers by recrystallization or chromatography and liberation of the optically pure product from the auxiliary, (2) salt formation employing an optically active resolving agent, or (3) direct separation of the mixture of optical enantiomers on chiral chromatographic columns. Stereoisomeric mixtures can also be resolved into their component stereoisomers by well-known methods, such as chiral-phase gas chromatography, chiral-phase high performance liquid chromatography, crystallizing the compound as a chiral salt complex, or crystallizing the compound in a chiral solvent. Further, enantiomers can be separated using supercritical fluid chromatographic (SFC) techniques described in the literature. Still further, stereoisomers can be obtained from stereomerically-pure intermediates, reagents, and catalysts by well-known asymmetric synthetic methods.
Geometric isomers can also exist in the compounds of the present invention. The symbol denotes a bond that may be a single, double or triple bond as described herein. The present invention encompasses the various geometric isomers and mixtures thereof resulting from the arrangement of substituents around a carbon-carbon double bond or arrangement of substituents around a carbocyclic ring. Substituents around a carbon-carbon double bond are designated as being in the “Z” or “E” configuration wherein the terms “Z” and “E” are used in accordance with IUPAC standards. Unless otherwise specified, structures depicting double bonds encompass both the “E” and “Z” isomers.
Substituents around a carbon-carbon double bond alternatively can be referred to as “cis” or “trans,” where “cis” represents substituents on the same side of the double bond and “trans” represents substituents on opposite sides of the double bond. The arrangement of substituents around a carbocyclic ring are designated as “cis” or “trans.” The term “cis” represents substituents on the same side of the plane of the ring and the term “trans” represents substituents on opposite sides of the plane of the ring. Mixtures of compounds wherein the substituents are disposed on both the same and opposite sides of plane of the ring are designated “cis/trans.”
The invention also embraces isotopically labeled compounds of the invention which are identical to those recited herein, except that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature. Examples of isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, fluorine and chlorine, such as 2H, 3H, 13C, 14C, 15N, 18O, 17O, 31P, 32P, 35S, 18F, and 36Cl, respectively.
Certain isotopically-labeled disclosed compounds (e.g., those labeled with 3H and 14C) are useful in compound and/or substrate tissue distribution assays. Tritiated (i.e., 3H) and carbon-14 (i.e., 14C) isotopes are particularly preferred for their ease of preparation and detectability. Further, substitution with heavier isotopes such as deuterium (i.e., 2H) may afford certain therapeutic advantages resulting from greater metabolic stability (e.g., increased in vivo half-life or reduced dosage requirements) and hence may be preferred in some circumstances. Isotopically labeled compounds of the invention can generally be prepared by following procedures analogous to those disclosed in, e.g., the Examples herein by substituting an isotopically labeled reagent for a non-isotopically labeled reagent.
As used herein, the terms “subject” and “patient” refer to organisms to be treated by the methods of the present invention. Such organisms are preferably mammals (e.g., murines, simians, equines, bovines, porcines, canines, felines, and the like), and more preferably humans.
The term “effective amount” refers to the amount of a compound (e.g., a compound of the present invention) or composition containing the compound sufficient to effect beneficial or desired results material. The term “therapeutically effective amount” refers to the amount of a compound (e.g., a compound of the present invention) or composition containing the compound effective for producing some desired therapeutic effect in at least a sub-population of cells in either a subject with or at risk of developing a LSD or an animal at a reasonable benefit/risk ratio applicable to any medical treatment. An effective amount or therapeutically effective amount can be administered in one or more administrations, applications or dosages and is not intended to be limited to a particular formulation or administration route.
The term “treating” refers any effect, e.g., lessening, reducing, modulating, ameliorating, reversing or eliminating, that results in the improvement of the condition, disease, disorder, and the like, or ameliorating a symptom thereof.
The term “pharmaceutical composition” refers to the combination of an active agent with a carrier, inert or active, making the composition especially suitable for diagnostic or therapeutic use in vivo or ex vivo.
The term “pharmaceutically acceptable” as used herein refers to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.
As used herein, the term “pharmaceutically acceptable carrier” refers to any of the standard pharmaceutical carriers, such as a phosphate buffered saline solution, water, emulsions (e.g., such as an oil/water or water/oil emulsions), and various types of wetting agents. The compositions also can include stabilizers and preservatives. For examples of carriers, stabilizers and adjuvants, see Martin, Remington's Pharmaceutical Sciences, 15th Ed., Mack Publ. Co., Easton, Pa. [1975].
As used herein, the term “pharmaceutically acceptable salt” refers to any pharmaceutically acceptable salt (e.g., acid or base) of a compound of the present invention which, upon administration to a subject, is capable of providing a compound of this invention or an active metabolite or residue thereof. As is known to those of skill in the art, “salts” of the compounds of the present invention may be derived from inorganic or organic acids and bases. Examples of acids include, but are not limited to, hydrochloric, hydrobromic, sulfuric, nitric, perchloric, fumaric, maleic, phosphoric, glycolic, lactic, salicylic, succinic, toluene-p-sulfonic, tartaric, acetic, citric, methanesulfonic, ethanesulfonic, formic, benzoic, malonic, naphthalene-2-sulfonic, benzenesulfonic acid, and the like. Other acids, such as oxalic, while not in themselves pharmaceutically acceptable, may be employed in the preparation of salts useful as intermediates in obtaining the compounds of the invention and their pharmaceutically acceptable acid addition salts.
Examples of bases include, but are not limited to, alkali metal (e.g., sodium) hydroxides, alkaline earth metal (e.g., magnesium) hydroxides, ammonia, and compounds of formula NW4+, wherein W is C1-4 alkyl, and the like.
Examples of salts include, but are not limited to: acetate, adipate, alginate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, camphorsulfonate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, fumarate, flucoheptanoate, glycerophosphate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, lactate, maleate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, oxalate, palmoate, pectinate, persulfate, phenylpropionate, picrate, pivalate, propionate, succinate, tartrate, thiocyanate, tosylate, undecanoate, and the like. Other examples of salts include anions of the compounds of the present invention compounded with a suitable cation such as Na+, NH4+, and NW4+ (wherein W is a C1-4 alkyl group), and the like.
For therapeutic use, salts of the compounds of the present invention are contemplated as being pharmaceutically acceptable. However, salts of acids and bases that are non-pharmaceutically acceptable may also find use, for example, in the preparation or purification of a pharmaceutically acceptable compound.
The terms “parenteral administration” and “administered parenterally” as used herein means modes of administration other than enteral and topical administration, usually by injection, and includes, without limitation, intravenous, intramuscular, intraarterial, intrathecal, intracapsular, intraorbital, intracardiac, intradermal, intraperitoneal, transtracheal, subcutaneous, subcuticular, intraarticulare, subcapsular, subarachnoid, intraspinal and intrasternal injection and infusion.
Abbreviations as used herein include O-(7-azabenzotriazol-1-yl)-N,N,N′N-tetramethyluronium hexafluorophosphate (HATU); diisopropylethylamine (DIPEA); dimethylformamide (DMF); methylene chloride (DCM); tert-butoxycarbonyl (Boc); tetrahydrofuran (THF); trifluoroacetic acid (TFA); N-methylmorpholine (NMM); triethylamine (TEA); Boc anhydride ((Boc)2O); dimethylsulfoxide (DMSO); diisopropylethylamine (DIEA); N,N-Dimethylpyridin-4-amine (DMAP); flash column chromatography (FCC); and supercritical fluid chromatography (SFC).
Throughout the description, where compositions and kits are described as having, including, or comprising specific components, or where processes and methods are described as having, including, or comprising specific steps, it is contemplated that, additionally, there are compositions and kits of the present invention that consist essentially of, or consist of, the recited components, and that there are processes and methods according to the present invention that consist essentially of, or consist of, the recited processing steps.
As a general matter, compositions specifying a percentage are by weight unless otherwise specified. Further, if a variable is not accompanied by a definition, then the previous definition of the variable controls.
The invention provides a method for treating a LSD in a subject in need thereof. The method comprises administering to the subject an effective amount of an acid ceramidase inhibitor sufficient to treat the disorder in the subject. The following section describes acid ceramidase inhibitors useful in the practice of the invention when administered, either alone or in combination with other agents, to the subject in need of such treatment. It is contemplated that this approach can be useful in treating Gaucher's disease, Krabbe disease, Fabry disease or Tay-Sachs disease, Sandhoff Variant AB disease, Niemann-Pick types A and B. It is contemplated that any of the acid ceramidase inhibitors set forth in Section III can be used to treat a LSD, in particular Gaucher's disease, Krabbe disease, Fabry disease or Tay-Sachs disease, Sandhoff Variant AB disease, Niemann-Pick types A and B.
For example, in connection with the treatment of Gaucher's disease (see,
Similarly, in connection with the treatment of Fabry's disease (see,
Similarly, in connection with the treatment of Krabbe's disease (see,
Similarly, in connection with the treatment of Tay-Sachs disease (or Sandhoff Variant AB), (see,
Similarly, in connection with the treatment of Niemann-Pick disease, types A and B (see,
Under certain circumstances, the acid ceramidase inhibitor, when administered to a subject, does not result in complete inhibition of the target acid ceramidase activity. Rather the amount of the acid ceramidase inhibitor is titrated to permit the target ceramidase to synthesize a sufficient amount of the sphingosine-containing analog for normal cellular function. In other words, the acid ceramidase inhibitor preferentially prevents an accumulation of the sphingosine-containing analog to abnormal levels, which become detrimental to cells and cellular function. The ceramidase inhibitor preferably reduces activity of the target ceramidase in a cell or tissue sample by less than 80%, 70%, 60%, 50%, 40%, 30%, 20%, 10% or 5% relative to activity prior to exposure by the inhibitor as determined by an in vitro assay, such as a fluorogenic assay employing a fluorogenic substrate, for example, Rbm14-12 (Bedia et al. (2010), supra). Furthermore, the acid ceramidase inhibitor can be titrated to permit the conversion of ceramide to sphingosine to provide normal or substantially normal levels of sphingosine in the subject. This can be accomplished by titrating the dosage of the inhibitor to establish the appropriate inhibition of acid ceramidase activity in the subject. This can be accomplished by employing a fluorogenic assay, for example, a fluorogenic assay using the fluorogenic substrate Rbm14-12 (Bedia et al. (2010), supra) to measure ceramidase activity in peripheral blood mononuclear cells extracted from the subject.
It is contemplated that a variety of acid ceramidase inhibitors can be used in the methods described herein.
It is contemplated that a variety of acid ceramidase inhibitors can be used in the practice of the invention. Exemplary acid ceramidase inhibitors can be tested for activity using a variety of in vitro assays known in the art, for example, as described in Bedia et al. (2010) supra. An exemplary assay may use a fluorogenic substrate as shown in Formula II
where different fatty acid chain lengths as denoted by integer n, which can be, for example, 6, 8, 10, 12, 14, 16, or 18. Exemplary fluorogenic analogs represented by Formula II include Rbm 14-10, Rbm 14-12, Rbm 14-14, and Rbm 14-16, where n can be 8, 10, 12, or 14, respectively, where Rbm 14-12 is preferred (Formula II, where n=8) (see, Bedia et al. (2010) supra). It is contemplated that exemplary acid ceramidase inhibitors reduce acid ceramidase activity by at least 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or 95% in the assay set forth in Bedia et al. (2010) supra using the fluorogenic Rbm 14-12 substrate.
Exemplary acid ceramidase inhibitors are described in Realini et al. (2013) S
In one embodiment, an exemplary acid ceramidase inhibitor is a compound of Formula I:
or a pharmaceutically acceptable salt thereof, wherein:
A1 is a cyclic group selected from 5-6 membered heterocyclyl, 5-6 membered heteroaryl, and bicyclic heterocyclyl, each of which is substituted by 1, 2, 3, or 4 occurrences of R2;
R1 represents independently for each occurrence hydrogen, C1-4alkyl, —C1-4alkyl-phenyl, —CO2—C1-6alkyl, —C(O)—NH2, —C(O)—NH—C1-6alkyl, or —C(O)—N(C1-6alkyl)2;
R2 represents independently for each occurrence R1, C1-4alkyl, C1-4haloalkyl, C1-4 alkoxy, halogen, hydroxyl, oxo, cyano, nitro, azido, —N(R1)2, —C(O)—C1-4alkyl, —C(O)-phenyl, —CO2—R1, —C(O)—NH2, —C(O)—NH—C1-6alkyl, —C(O)—N(C1-6alkyl)2, —O—C(O)—NH2, —O—C(O)—NH—C1-6alkyl, —O—C(O)—N(C1-6alkyl)2, —C1-4alkyl-phenyl, C3-10cycloalkyl, C3-10heterocyclyl, 6-10 membered aryl, 6-10 membered heteroaryl, —C1-4alkylene-C3-10cycloalkyl, —C1-4alkylene-C3-10 heterocyclyl, —(C1-4alkylene)-6-10 membered aryl, or —(C1-4alkylene)-6-10 membered heteroaryl;
Y1 represents:
W1 represents:
Definitions of the variables in Formula I above encompass multiple chemical groups. The application contemplates embodiments where, for example, i) the definition of a variable is a single chemical group selected from those chemical groups set forth above, ii) the definition is a collection of two or more of the chemical groups selected from those set forth above, and iii) the compound is defined by a combination of variables in which the variables are defined by (i) or (ii), e.g., such as where Y1 is C1-18alkylene, W1 is 6-10 membered arylene, and A1 is bicyclic heterocyclyl.
In certain embodiments, R1 represents hydrogen.
In certain embodiments, R2 represents independently for each occurrence hydrogen, C1-4alkyl, —C1-4-phenyl, phenyl, halophenyl, —C(O)—C1-4alkyl, methyl, isopropyl, fluoro, chloro, bromo, C1-4haloalkyl, or trifluoromethyl.
In certain embodiments, Y1 is C1-18alkylene. For example, in certain embodiments, Y1 may be C1-6alkylene, C1-4alkylene, methylene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene, or nonylene, decylene, undecylene, or dodecylene. In certain embodiments, Y1 is 6-10 membered arylene. For example, in certain embodiments, Y1 may be indanylene or tetralinylene.
In certain embodiments, W1 is C3-10cycloalkylene, C3-10heterocyclylene, 6-10 membered arylene, or 6-10 membered heteroarylene, each of which may be substituted with one, two, or three occurrences of C1-6alkyl or C1-6alkoxy. In certain embodiments, W1 is hydrogen, phenyl, methylphenyl, dimethylphenyl, cyclohexyl, methoxyphenyl, dimethoxyphenyl, or trimethoxyphenyl. In certain embodiments, W1 is 6-10 membered arylene. For example, in certain embodiments, W1 may be indanylene or tetralinylene.
In certain embodiments, A1 is furanyl, pyrrolyl, thiophenyl, pyrazolyl, oxazolyl, thiazolyl, pyridinyl, pyrimidinyl, tetrahydropyrimidinyl, pyrazinyl, dihydroisooxazolyl, isooxazolyl, isothiazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, imidazolinyl, imidazolidinyl, oxazolinyl, pyrazolinyl, thiazolinyl, triazolinyl, dihydrobenzooxazolyl, dihydrobenzoisoxazole, dihydrobenzothiazolyl, dihydrooxazolopyridinyl, dihydroimidazopyridinyl, dihydropyrazolopyridinyl, dihydroindazolyl, dihydrobenzoisothiazolyl, dihydroisothiazolopyridine, indazolyl, benzotriazolyl, or triazolopyridine. In certain embodiments, A1 is furanyl, pyrrolyl, thiophenyl, pyrazolyl, oxazolyl, thiazolyl, pyridinyl, pyrimidinyl, tetrahydropyrimidinyl, pyrazinyl, dihydroisooxazolyl, isooxazolyl, isothiazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, imidazolinyl, imidazolidinyl, oxazolinyl, pyrazolinyl, thiazolinyl, triazolinyl, dihydrobenzooxazolyl, dihydrobenzoisoxazole, dihydrobenzothiazolyl, dihydrooxazolopyridinyl, dihydroimidazopyridinyl, dihydropyrazolopyridinyl, dihydroindazolyl, dihydrobenzoisothiazolyl, dihydroisothiazolopyridine, indazolyl, benzotriazolyl, or triazolopyridine, each of which is substituted by one, two, three, or four substituents independently selected from R2.
In certain embodiments, A1 is
wherein n is 0, 1, 2, 3, or 4.
In certain embodiments, the acid ceramidase inhibitor is a compound of Formula I-1:
or a pharmaceutically acceptable salt thereof, wherein:
A1 is a cyclic group selected from 5-6 membered heterocyclyl, 5-6 membered heteroaryl, and bicyclic heterocyclyl, each of which is substituted by 1, 2, or 3 occurrences of R2;
R1 represents independently for each occurrence hydrogen, C1-4alkyl, —C1-4alkyl-phenyl, —CO2—C1-6alkyl, —C(O)—NH2, —C(O)—NH—C1-6alkyl, or —C(O)—N(C1-6alkyl)2;
R2 represents independently for each occurrence R1, C1-4alkyl, C1-4haloalkyl, C1-4 alkoxy, halogen, hydroxyl, oxo, cyano, nitro, azido, —N(R1)2, —C(O)—C1-4alkyl, —C(O)-phenyl, —CO2—R1, —C(O)—NH2, —C(O)—NH—C1-6alkyl, —C(O)—N(C1-6alkyl)2, —O—C(O)—NH2, —O—C(O)—NH-C1-6alkyl, —O—C(O)—N(C1-6alkyl)2, —C1-4alkyl-phenyl, C3-10cycloalkyl, C3-10heterocyclyl, 6-10 membered aryl, 6-10 membered heteroaryl, —C1-4alkylene-C3-10cycloalkyl, —C1-4alkylene-C3-10 heterocyclyl, —C1-4alkylene-6-10 membered aryl, or —C1-4alkylene-6-10 membered heteroaryl;
Y1 represents:
W1 represents:
Definitions of the variables in Formula I-1 above encompass multiple chemical groups. The application contemplates embodiments where, for example, i) the definition of a variable is a single chemical group selected from those chemical groups set forth above, ii) the definition is a collection of two or more of the chemical groups selected from those set forth above, and iii) the compound is defined by a combination of variables in which the variables are defined by (i) or (ii), e.g., such as where Y1 is C1-18alkylene, W1 is 6-10 membered arylene, and A1 is bicyclic heterocyclyl.
In certain embodiments A1 is
wherein m is 0, 1, 2, 3.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In certain embodiments, an acid ceramidase inhibitor may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
Other contemplated acid ceramidase inhibitors may be selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
In one embodiment, an exemplary acid ceramidase inhibitor is a compound of Formula III:
or a pharmaceutically acceptable salt thereof, wherein:
X is O or S;
B is hydrogen, linear or branched C1-6 alkyl;
C is a linear or branched C5-12 alkyl group or a group:
wherein:
a is an integer from 1 to 6;
G is a 3-10 membered saturated, unsaturated, aromatic or heteroaromatic, single or fused ring comprising up to three heteroatoms selected from N, O, S; and Z4 and Z5 are as defined below;
Z1, Z2, Z3, Z4 and Z5, are independently selected from the group consisting of hydrogen, halogen, linear or branched C1-6 alkyl, optionally substituted cycloalkyl C1-6 alkyl, optionally substituted cycloalkyl C2-6 alkenyl, optionally substituted aryl C1-6 alkyl, optionally substituted aryl C1-6 alkenyl, C1-6 alkoxy, optionally substituted cycloalkyl C1-6 alkoxy, optionally substituted aryl C1-6 alkoxy, hydroxy C1-6 alkyl, OH, CN, NO2, fluoro C1-6 alkyl, fluoro C1-6 alkoxy, optionally substituted aryl, C1-6 alkylCO, optionally substituted arylCO, optionally substituted aryl C1-6 alkylCO, COOZ7, CONZ8Z9, SO2Z10;
wherein Z7, Z8, Z9 and Z10 are independently selected from the group consisting of hydrogen, linear or branched C1-6 alkyl;
Z1, Z2, Z3, Z4 and Z5 can be attached to any position of the ring to which they are connected.
In certain embodiments, compounds of Formula (III) as defined above are provided wherein:
X is O or S;
B is hydrogen or a linear or branched C1-6 alkyl;
C is a linear or branched C5-12 alkyl group or a group:
wherein:
a is an integer from 1 to 6;
G is
Z1, Z2, Z3, Z4 and Z5, are independently selected from the group consisting of hydrogen, halogen, linear or branched C1-6 alkyl, optionally substituted cycloalkyl C1-6 alkyl, optionally substituted cycloalkyl C2-6 alkenyl, optionally substituted aryl C1-6 alkyl, optionally substituted aryl C2-6 alkenyl, C1-6 alkoxy, optionally substituted cycloalkyl C1-6 alkoxy, optionally substituted aryl C1-6 alkoxy, hydroxy C1-6 alkyl, OH, CN, NO2, fluoro C1-6 alkyl, fluoro C1-6 alkoxy, optionally substituted aryl, C1-6 alkylCO, optionally substituted arylCO, optionally substituted aryl C1-6 alkylCO, COOZ7, CONZ8Z9, SO2Z10;
wherein Z7, Z8, Z9 and Z10 are independently selected from the group consisting of hydrogen, linear or branched C1-6 alkyl;
wherein Z1, Z2, Z3, Z4 and Z5 can be attached to any position of the ring to which they are connected.
In certain embodiments, compounds of Formula (III) as defined above are provided wherein:
X is O or S;
B is hydrogen or a linear or branched C1-6 alkyl;
C is a linear or branched C5-9 alkyl group or a group:
wherein:
a is an integer from 1 to 6;
G is an aryl selected from naphthyl or phenyl, (C3-C10)cycloalkyl, a heteroaryl which is pyridyl, thiophenyl, pyrimidinyl, furyl, indolyl;
wherein Z4 and Z5, if present, independently are halogen, NO2, (C1-C3)alkoxy-, (C3-C10) cycloalkyl, linear or branched C1-C6 alkyl;
Z4 and Z5 can be attached to any position of the ring to which they are connected;
Z1, Z2, Z3, are independently (i) hydrogen, halogen, linear or branched C1-6 alkyl, OH, CN, NO2, fluoro C1-6 alkyl, hydroxy C1-6 alkyl; (ii) phenyl optionally substituted with C1-C6 alkyl, C1-C3 alkoxy, C2-C6 alkenyl, halogen, NO2, CF3; (iii) phenyl C1-6 alkyl optionally substituted with C1-C6 alkyl, C1-C3 alkoxy, C2-C6 alkenyl, halogen, NO2, CF3; (iv) phenyl C2-6 alkenyl optionally substituted with C1-C6 alkyl, C1-C3 alkoxy, C2-C6 alkenyl, halogen, NO2, CF3; (v) phenyl CO optionally substituted with C1-C6 alkyl, C1-C3 alkoxy, C2-C6 alkenyl, halogen, NO2, CF3; (vi) C1-C6 alkyl CO optionally substituted with phenyl, optionally substituted with C1-C6 alkyl, C1-C3 alkoxy, C2-C6 alkenyl, halogen, NO2, CF3; (vii) (C3-C10)cycloalkyl C1-6 alkyl optionally substituted with C1-C6 alkyl, C2-C6 alkenyl, halogen; (viii) (C3-C10)cycloalkyl C24 alkenyl optionally substituted with C1-C6 alkyl, C2-C6 alkenyl, halogen; or (iX) C1-6 alkoxy optionally substituted with halogen, (C3-C10)cycloalkyl, phenyl;
wherein Z1, Z2, or Z3 can be attached to any position of the ring to which they are connected.
In certain embodiments, compounds of Formula (III) as defined above are provided wherein:
X is O;
B is hydrogen;
C is a linear or branched C5-9 alkyl group or preferably a group:
wherein:
a is an integer from 1 to 4;
G is phenyl, thiophenyl, pyridyl, naphthyl or C3-7 cycloalkyl, preferably cyclohexyl;
Z1, Z2, Z3, Z4 and Z5, are, independently, H, F, Cl, Br, Me, Et, Pr, MeO, BuO, OH, CN, NO2, CF3, Ph, MeCO, or EtCO;
wherein Z1, Z2, Z3, Z4 and Z5 can be attached to any position of the ring to which they are connected.
Exemplary compounds of Formula III are set forth in Table 2.
In one embodiment, an exemplary acid ceramidase inhibitor is a compound of Formula IV:
or a pharmaceutically acceptable salt thereof, wherein:
L is a bond, CO, CH(OH) or CH2;
L can be attached to any position of the ring to which it connected;
Q, V1 and V2 are independently hydrogen, linear or branched C1-6 alkyl;
s is an integer from 1 to 6;
J is a linear or branched C1-9 alkyl, C2-9 alkenyl or C2-9 alkynyl group or a group:
wherein:
p is 0 or an integer from 1 to 6;
U is a 3-10 membered saturated, unsaturated, aromatic or heteroaromatic, single or fused ring comprising up to three heteroatoms selected from N, O, S; and V6 and V7 are as defined below;
V3 is hydrogen, halogen, linear or branched C1-6 alkyl, C1-6 alkoxy or OH;
V3 can be attached to any position of the ring to which it is connected;
V4 and V5 are independently selected from the group consisting of hydrogen, halogen, linear or branched C1-6 alkyl, C1-6 alkoxy, hydroxy C1-6 alkyl, OH, CN, NO2, fluoro C1-6 alkyl, fluoro C1-6 alkoxy, COOV8, CONV9V10, SO2NV9V10, SO2V11;
V6 and V7 are independently selected from the group consisting of hydrogen, halogen, linear or branched C1-6 alkyl, optionally substituted C3-6 cycloalkyl, C1-6 alkoxy, hydroxy C1-6 alkyl, OH, CN, NO2, fluoro C1-6 alkyl, fluoro C1-6 alkoxy, optionally substituted aryl or heteroaryl, COOV8, CONV9V10, SO2NV9V10, SO2V11;
V4, V5, V6 and V7 can be attached to any position of the ring to which they are connected;
E is a bond or a heteroatom selected from the group consisting of O, S, SO, SO2 or NV12;
V8, V9, V10, V11 and V12 are independently selected from the group consisting of hydrogen, linear or branched C1-6 alkyl;
provided that when E is a bond, both the following conditions are met:
J is a group:
and s+p is >4.
In certain embodiments, compounds of Formula (IV) as defined above are provided wherein:
L is a bond, CO, CH(OH);
Q is hydrogen;
V1 and V2 are independently hydrogen, linear or branched C1-6 alkyl, preferably methyl;
s is an integer from 1 to 6;
J is a linear C1-6 alkyl or a group:
p is an integer from 1 to 6;
U is an aryl selected from naphthyl or phenyl, (C3-C10)cycloalkyl, or a heteroaryl which is pyridyl, thiophenyl, pyrimidinyl, furyl, or indolyl;
V3 is hydrogen, halogen, preferably chlorine or fluorine;
V4 and V5 are independently selected from the group consisting of hydrogen, halogen preferably F, linear or branched C1-6 alkyl preferably C1-3 alkyl, C1-6 alkoxy preferably MeO and EtO, OH, CN, NO2, CF3, hydroxy C1-6 alkyl;
V6 and V7 are independently selected from the group consisting of hydrogen, halogen, linear or branched C1-6 alkyl, C1-6 alkoxy, preferably MeO and EtO, hydroxy C1-6 alkyl, OH, CN, NO2, CF3; preferably both V6 and V7 are hydrogen;
E is a bond or a heteroatom selected from the group consisting of O, S, SO, SO2;
with the proviso that when E is a bond, J is a group:
and s+p is >4.
Exemplary compounds of Formula IV are set forth in Table 3.
The invention embraces combination therapy, which includes the administration of an acid ceramidase inhibitor and a second agent as part of a specific treatment regimen intended to provide the beneficial effect from the co-action of these therapeutic agents. The beneficial effect of the combination may include pharmacokinetic or pharmacodynamic co-action resulting from the combination of therapeutic agents.
Exemplary second agents for use in treating Gaucher disease include, for example, imiglucerase (CEREZYME®), taliglucerase alfa (ELELYSO®), velaglucerase alfa (VPRIV®), eliglustat (CERDELGA®), and miglustat (ZAVESCA®) or a glucocerebrosidase activator such as one or more of the compounds described in International Application Publication No. WO2012/078855. Exemplary second agents for use in treating Fabry disease include, for example, alpha-galactosidase A (FABRAZYME®).
The acid ceramidase inhibitors described hereinabove useful in the treatment of LSDs can be present in a pharmaceutical composition. In certain embodiments, the pharmaceutical compositions preferably comprise a therapeutically-effective amount of one or more of the acid ceramidase inhibitors described above formulated together with one or more pharmaceutically acceptable carriers. As described in detail below, the pharmaceutical compositions of the present invention may be specially formulated for administration in solid or liquid form, including those adapted for the following: (1) oral administration, for example, drenches (aqueous or non-aqueous solutions or suspensions), tablets (e.g., those targeted for buccal, sublingual, and/or systemic absorption), boluses, powders, granules, pastes for application to the tongue; (2) parenteral administration by, for example, subcutaneous, intramuscular, intravenous or epidural injection as, for example, a sterile solution or suspension, or sustained-release formulation; (3) topical application, for example, as a cream, ointment, or a controlled-release patch or spray applied to the skin; (4) intravaginally or intrarectally, for example, as a pessary, cream or foam; (5) sublingually; (6) ocularly; (7) transdermally; or (8) nasally.
Wetting agents, emulsifiers and lubricants, such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, release agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the compositions.
Examples of pharmaceutically-acceptable antioxidants include: (1) water soluble antioxidants, such as ascorbic acid, cysteine hydrochloride, sodium bisulfate, sodium metabisulfite, sodium sulfite and the like; (2) oil-soluble antioxidants, such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin, propyl gallate, alpha-tocopherol, and the like; and (3) metal chelating agents, such as citric acid, ethylenediamine tetraacetic acid (EDTA), sorbitol, tartaric acid, phosphoric acid, and the like.
Formulations of the present invention include those suitable for oral, nasal, topical (including buccal and sublingual), rectal, vaginal and/or parenteral administration. The formulations may conveniently be presented in unit dosage form and may be prepared by any methods well known in the art of pharmacy. The amount of active ingredient which can be combined with a carrier material to produce a single dosage form will vary depending upon the host being treated, the particular mode of administration.
The amount of active ingredient which can be combined with a carrier material to produce a single dosage form will generally be that amount of the compound which produces a therapeutic effect. Generally, out of one hundred percent, this amount will range from about 0.1 percent to about ninety-nine percent of active ingredient, preferably from about 5 percent to about 70 percent, most preferably from about 10 percent to about 30 percent.
In certain embodiments, a formulation of the present invention comprises an excipient selected from the group consisting of cyclodextrins, celluloses, liposomes, micelle forming agents, e.g., bile acids, and polymeric carriers, e.g., polyesters and polyanhydrides; and a compound of the present invention. In certain embodiments, an aforementioned formulation renders orally bioavailable a compound of the present invention.
Methods of preparing these formulations or compositions include the step of bringing into association a compound of the present invention with the carrier and, optionally, one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing into association a compound of the present invention with liquid carriers, or finely divided solid carriers, or both, and then, if necessary, shaping the product.
Formulations of the invention suitable for oral administration may be in the form of capsules, cachets, pills, tablets, lozenges (using a flavored basis, usually sucrose and acacia or tragacanth), powders, granules, or as a solution or a suspension in an aqueous or non-aqueous liquid, or as an oil-in-water or water-in-oil liquid emulsion, or as an elixir or syrup, or as pastilles (using an inert base, such as gelatin and glycerin, or sucrose and acacia) and/or as mouth washes and the like, each containing a predetermined amount of a compound of the present invention as an active ingredient. A compound of the present invention may also be administered as a bolus, electuary or paste.
In solid dosage forms of the invention for oral administration (capsules, tablets, pills, dragees, powders, granules, trouches and the like), the active ingredient is mixed with one or more pharmaceutically-acceptable carriers, such as sodium citrate or dicalcium phosphate, and/or any of the following: (1) fillers or extenders, such as starches, lactose, sucrose, glucose, mannitol, and/or silicic acid; (2) binders, such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinyl pyrrolidone, sucrose and/or acacia; (3) humectants, such as glycerol; (4) disintegrating agents, such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate; (5) solution retarding agents, such as paraffin; (6) absorption accelerators, such as quaternary ammonium compounds and surfactants, such as poloxamer and sodium lauryl sulfate; (7) wetting agents, such as, for example, cetyl alcohol, glycerol monostearate, and non-ionic surfactants; (8) absorbents, such as kaolin and bentonite clay; (9) lubricants, such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, zinc stearate, sodium stearate, stearic acid, and mixtures thereof; (10) coloring agents; and (11) controlled release agents such as crospovidone or ethyl cellulose. In the case of capsules, tablets and pills, the pharmaceutical compositions may also comprise buffering agents. Solid compositions of a similar type may also be employed as fillers in soft and hard-shelled gelatin capsules using such excipients as lactose or milk sugars, as well as high molecular weight polyethylene glycols and the like.
A tablet may be made by compression or molding, optionally with one or more accessory ingredients. Compressed tablets may be prepared using binder (for example, gelatin or hydroxypropylmethyl cellulose), lubricant, inert diluent, preservative, disintegrant (for example, sodium starch glycolate or cross-linked sodium carboxymethyl cellulose), surface-active or dispersing agent. Molded tablets may be made by molding in a suitable machine a mixture of the powdered compound moistened with an inert liquid diluent.
The tablets, and other solid dosage forms of the pharmaceutical compositions of the present invention, such as dragees, capsules, pills and granules, may optionally be scored or prepared with coatings and shells, such as enteric coatings and other coatings well known in the pharmaceutical-formulating art. They may also be formulated so as to provide slow or controlled release of the active ingredient therein using, for example, hydroxypropylmethyl cellulose in varying proportions to provide the desired release profile, other polymer matrices, liposomes and/or microspheres. They may be formulated for rapid release, e.g., freeze-dried. They may be sterilized by, for example, filtration through a bacteria-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved in sterile water, or some other sterile injectable medium immediately before use. These compositions may also optionally contain opacifying agents and may be of a composition that they release the active ingredient(s) only, or preferentially, in a certain portion of the gastrointestinal tract, optionally, in a delayed manner. Examples of embedding compositions which can be used include polymeric substances and waxes. The active ingredient can also be in micro-encapsulated form, if appropriate, with one or more of the above-described excipients.
Liquid dosage forms for oral administration of the compounds of the invention include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. In addition to the active ingredient, the liquid dosage forms may contain inert diluents commonly used in the art, such as, for example, water or other solvents, solubilizing agents and emulsifiers, such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor and sesame oils), glycerol, tetrahydrofuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof.
Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, coloring, perfuming and preservative agents.
Suspensions, in addition to the active compounds, may contain suspending agents as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth, and mixtures thereof.
Formulations of the pharmaceutical compositions of the invention for rectal or vaginal administration may be presented as a suppository, which may be prepared by mixing one or more compounds of the invention with one or more suitable nonirritating excipients or carriers comprising, for example, cocoa butter, polyethylene glycol, a suppository wax or a salicylate, and which is solid at room temperature, but liquid at body temperature and, therefore, will melt in the rectum or vaginal cavity and release the active compound.
Formulations of the present invention which are suitable for vaginal administration also include pessaries, tampons, creams, gels, pastes, foams or spray formulations containing such carriers as are known in the art to be appropriate.
Dosage forms for the topical or transdermal administration of a compound of this invention include powders, sprays, ointments, pastes, creams, lotions, gels, solutions, patches and inhalants. The active compound may be mixed under sterile conditions with a pharmaceutically-acceptable carrier, and with any preservatives, buffers, or propellants which may be required.
The ointments, pastes, creams and gels may contain, in addition to an active compound of this invention, excipients, such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.
Powders and sprays can contain, in addition to a compound of this invention, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances. Sprays can additionally contain customary propellants, such as chlorofluorohydrocarbons and volatile unsubstituted hydrocarbons, such as butane and propane.
Transdermal patches have the added advantage of providing controlled delivery of a compound of the present invention to the body. Such dosage forms can be made by dissolving or dispersing the compound in the proper medium. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate of such flux can be controlled by either providing a rate controlling membrane or dispersing the compound in a polymer matrix or gel.
Ophthalmic formulations, eye ointments, powders, solutions and the like, are also contemplated as being within the scope of this invention.
Pharmaceutical compositions of this invention suitable for parenteral administration comprise one or more compounds of the invention in combination with one or more pharmaceutically-acceptable sterile isotonic aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, or sterile powders which may be reconstituted into sterile injectable solutions or dispersions just prior to use, which may contain sugars, alcohols, antioxidants, buffers, bacteriostats, solutes which render the formulation isotonic with the blood of the intended recipient or suspending or thickening agents.
Examples of suitable aqueous and nonaqueous carriers which may be employed in the pharmaceutical compositions of the invention include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), and suitable mixtures thereof, vegetable oils, such as olive oil, and injectable organic esters, such as ethyl oleate. Proper fluidity can be maintained, for example, by the use of coating materials, such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants.
These compositions may also contain adjuvants such as preservatives, wetting agents, emulsifying agents and dispersing agents. Prevention of the action of microorganisms upon the subject compounds may be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It may also be desirable to include isotonic agents, such as sugars, sodium chloride, and the like into the compositions. In addition, prolonged absorption of the injectable pharmaceutical form may be brought about by the inclusion of agents which delay absorption such as aluminum monostearate and gelatin.
In some cases, in order to prolong the effect of a drug, it is desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This may be accomplished by the use of a liquid suspension of crystalline or amorphous material having poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution which, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally-administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle.
Injectable depot forms are made by forming microencapsule matrices of the subject compounds in biodegradable polymers such as polylactide-polyglycolide. Depending on the ratio of drug to polymer, and the nature of the particular polymer employed, the rate of drug release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions which are compatible with body tissue.
When the compounds of the present invention are administered as pharmaceuticals, to humans and animals, they can be given per se or as a pharmaceutical composition containing, for example, 0.1 to 99% (more preferably, 10 to 30%) of active ingredient in combination with a pharmaceutically acceptable carrier.
The preparations of the present invention may be given orally, parenterally, topically, or rectally. They are of course given in forms suitable for each administration route. For example, they are administered in tablets or capsule form, by injection, inhalation, eye lotion, ointment, suppository, etc. administration by injection, infusion or inhalation; topical by lotion or ointment; and rectal by suppositories. Oral administrations are preferred.
These compounds may be administered to humans and other animals for therapy by any suitable route of administration, including orally, nasally, as by, for example, a spray, rectally, intravaginally, parenterally, intracisternally and topically, as by powders, ointments or drops, including buccally and sublingually.
Regardless of the route of administration selected, the compounds of the present invention, which may be used in a suitable hydrated form, and/or the pharmaceutical compositions of the present invention, are formulated into pharmaceutically-acceptable dosage forms by conventional methods known to those of skill in the art.
Actual dosage levels of the active ingredients in the pharmaceutical compositions of this invention may be varied so as to obtain an amount of the active ingredient which is effective to achieve the desired therapeutic response for a particular patient, composition, and mode of administration, without being toxic to the patient.
The selected dosage level will depend upon a variety of factors including the activity of the particular compound of the present invention employed, or the ester, salt or amide thereof, the route of administration, the time of administration, the rate of excretion or metabolism of the particular compound being employed, the rate and extent of absorption, the duration of the treatment, other drugs, compounds and/or materials used in combination with the particular compound employed, the age, sex, weight, condition, general health and prior medical history of the patient being treated, and like factors well known in the medical arts.
A physician or veterinarian having ordinary skill in the art can readily determine and prescribe the effective amount of the pharmaceutical composition required. For example, the physician or veterinarian could start doses of the compounds of the invention employed in the pharmaceutical composition at levels lower than that required in order to achieve the desired therapeutic effect and gradually increase the dosage until the desired effect is achieved. In other words, a compound of the invention may be tritrated by a physician or veterinarian at escalating dosages to the subject over a period of days, weeks, or months to ameliorate at least one symptom associated with the LSD in question.
In general, a suitable daily dose of a compound of the invention will be that amount of the compound which is the lowest dose effective to produce a therapeutic effect. Such an effective dose will generally depend upon the factors described above. The compound or compounds can administered at about 0.01 mg/kg to about 200 mg/kg, at about 0.1 mg/kg to about 100 mg/kg, or at about 0.5 mg/kg to about 50 mg/kg. In certain embodiments, the compound or compounds can be administered at a concentration less than 20 mg/kg. When the compounds described herein are co-administered with another agent (e.g., as sensitizing agents), the effective amount may be less than when the agent is used alone.
If desired, the effective daily dose of the active compound may be administered as two, three, four, five, six or more sub-doses administered separately at appropriate intervals throughout the day, optionally, in unit dosage forms. Preferred dosing is one administration per day.
Another aspect of the invention provides a kit for treating a LSD. The kit comprises: (i) instructions for treating a medical disorder, such as Gaucher disease; and (ii) an acid ceramidase inhibitor. The kit may comprise one or more unit dosage forms containing an amount of an acid ceramidase inhibitor that is effective for treating the LSD, e.g., Gaucher disease.
This example describes the acid ceramidase inhibition activity of compound 25 of Table 2 (Formula III).
Inhibition of acid ceramidase activity by compound 25 of Table 2 was evaluated in a fluorescent intensity assay using a fluorogenic substrate Rbm 14-12 (RNA-binding protein 14-12). Compound 25 was incubated with cell lysates enriched with acid ceramidase for 1 hour in an assay buffer containing 50 mM NaOAc and 100 mM NaCl at pH 4.5. The reaction was initiated by the addition of the substrate at a final concentration of 6.3 μM and the mixture was incubated at room temperature for 1 or two hours. At the appropriate time, the reaction was quenched by the addition of methanol and treated with NaIO4 (fresh 2.5 mg/ml solution was made in 100 mM glycine/NaOH buffer, pH 10.6), followed by incubation for 1 hour at room temperature. Fluorescent intensity was measured using a plate reader at ex 355 nm and em 460 nm. The obtained average IC50 value for the 1 and 2 hour time points was in the range of 250 nM to 500 nM.
The entire disclosure of each of the patent documents and scientific articles referred to herein is incorporated by reference for all purposes.
The invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The foregoing embodiments are therefore to be considered in all respects illustrative rather than limiting the invention described herein. Scope of the invention is thus indicated by the appended claims rather than by the foregoing description, and all changes that come within the meaning and range of equivalency of the claims are intended to be embraced therein.
This application claims the benefit of and priority to U.S. Provisional Patent Application No. 62/184,508, filed Jun. 25, 2015, the contents of which are hereby incorporated by reference.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2016/038998 | 6/23/2016 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62184508 | Jun 2015 | US |
