Patent Application
20080242597
Infections caused by bacteria are a growing medical concern as many of these bacteria are resistant to various antibiotics. Such microbes include Staphylococcus aureus, Staphylococcus hemolyticus, Pediococcus spp., and Streptococcus pyogenes, Streptococcus pneumoniae, Pseudomonas aeruginosa, Vibrio cholerae, Vibrio parahemolyticus, Actinobacter calcoaeticus, Stenotrophomonas maltophilia.
Many thiazolyl peptide antibiotics exhibit potent antibacterial activity against a variety of Gram-positive bacteria, including multiple drug-resistant strains. Their poor water solubility severely limits their usage as therapeutic agents.
The present invention relates to novel sugar substituted thiazolyl peptide antibiotics capable of treating serious bacterial infections in mammals, and particularly, in humans. These analogs can also be versatile intermediates for the preparation of new derivatives with useful antibacterial activity. Many of the novel thiazolyl peptide antibiotics of the present invention show much improved aqueous solubility (see WO2004/004646, WO2002/14354, WO2002/13834, WO2000/68413, WO200014100, WO2000/03722, WO2002/66046 and PCT US2005/33326, filed Sep. 16, 2005). While some methods have been reported to improve the aqueous solubility of thiazolyl peptide antibiotics [see P. Hrnciar et al., J Org. Chem. 2002, 67(25), 8789-8793; B. Naidu, et al., Bioorganic & Med. Chem. Ltrs. (2004), 14(22), 5573-5577; M. Pucci, et al., Antimicrobial Agts. And Chemo., (2004), 48(10), 3697-3701; B. Naidu, et al, Tetrahedron Letters (2004), 45(17), 3531, and Tetrahedron Letters (2004), 45(5), 1059-1063; M. D. Lee et al., J. Antibiotics August 1994, Vol. 47 No. 8 pages 901-908; T. Otani et al., J. Antibiotics 1998, Vol. 51 No. 8, pages 715-721; and M. D. Lee et al., J. Antibiotics 1994, Vol. 47 No. 8 pages 894-900], the current invention uses a different approach targeting the sugar residue of the natural products. The antibiotics of this invention thus comprise an important contribution to therapy for treating infections which are resistant to various known antibiotics.
This invention is concerned with novel thiazolyl-peptide antibiotics of the formula I:
or a pharmaceutically acceptable salt, ester, enantiomer, diasteriomer or mixture thereof,
wherein:
R independently represents hydrogen, and C1-12 alkyl;
R1 represents hydrogen, C1-6 alkyl, and C3-6 cycloalkyl, —(CH2)nC5-10 heterocyclyl;
R2 represents R1 and OR1;
R3 represents —C(O)NR5R6, —C(O)NHC(R7R8)C(O)NR5R6, C(O)OR5;
R4 represents
R4a represents C1-12 alkyl, C(O)H, C(O)C1-12 alkyl, —C(R5)2C5-10 heterocyclyl , —COOR, —(CH2)nC(O)NR5R6, —(CH2)nNR5R6, —(CH2)nC5-10 heterocyclyl, —(CH2)nP(O)(OR)2, said aryl, and heterocyclyl optionally substituted with one or more groups of Ra; said alkyl optionally substituted with 1 to 6 hydroxy and/or optionally substituted by one or more groups of Ra; —
R5 and R6 independently represent hydrogen, C1-2 alkyl, —(CH2)nC(═CH2)C(O)NH2, —(CH2)nC(═CH2)CN, —(CH2)nC5-10 heterocyclyl, —(CH2)nNR7R8, CHO, —(CH2)nNR(CH2)nNR7R8, —(CH2)nNR(CH2)nC5-10 heterocyclyl, —(CH2)nC6-10 aryl, —(CH2)n(O(CH2)2)1-6R9, —(CH2)nNHC(O)(CH2)nNR7R8, said aryl, and heterocyclyl optionally substituted with one or more groups of Ra; said alkyl optionally substituted with 1 to 6 hydroxy and/or optionally substituted by one or more groups of Ra; or
R5 and R6 together with the nitrogen atom they are attached form a 5 to 10 heterocyclic ring optionally containing 1 to 2 additional heteroatoms selected from the group consisting of N, S and O and optionally substituted with one or more groups of Ra;
R7 and R8 independently represent hydrogen, —(CH2)nNR5R6, —(CH2)nSR5; —(CH2)nC5-10 heterocyclyl said heterocyclyl optionally substituted with one or more groups of Ra; said alkyl optionally substituted with 1 to 6 hydroxy and/or optionally substituted by one or more groups of Ra;
R9 represents hydrogen, C1-6 alkyl, (CH2)nC5-10 heterocyclyl, —C(O)OR, CN, OR, said alkyl and heterocyclyl optionally substituted with one or more groups of Ra
Ra represents hydrogen, halogen, (CH2)nOR, CF3, (CH2)nC(O)OR, (CH2)nC(O)NR7R8, (CH2)nC5-10 heterocyclyl, SO2NR5R6, (CH2)C6-10 aryl, N(R)2, NO2, CN, (C1-6 alkyl)O—, (aryl)O—, (C1-6 alkyl)S(O)0-2—, C1-12 alkyl, said alkyl, heterocyclyl, and aryl optionally substituted with 1 to 4 groups selected from the group consisting of C1-6 alkyl, (CH2)nOR, (CH2)nN(R)2, —O—; and
n represent 0-6, and p represents 0, 1 or 2.
The invention is described herein in detail using the terms defined below unless otherwise specified.
The compounds of the present invention may have asymmetric centers, chiral axes and chiral planes, and occur as racemates, racemic mixtures, and as individual diastereomers, with all possible isomers, including optical isomers, being included in the present invention. (See E. L. Eliel and S. H. Wilen Stereochemistry of Carbon Compounds (John Wiley and Sons, New York 1994), in particular pages 1119-1190).
When any variable (e.g. aryl, heterocycle, R4, R1 etc.) occurs more than one time in any constituent, its definition on each occurrence is independent at every other occurrence. Also, combinations of substituents/or variables are permissible only if such combinations result in stable compounds.
The term “alkyl” refers to a monovalent alkane (hydrocarbon) derived radical containing from 1 to 15 carbon atoms unless otherwise defined. It may be straight or branched. Preferred alkyl groups include lower alkyls which have from 1 to 6 carbon atoms such as methyl, ethyl, propyl, isopropyl, butyl and t-butyl. When substituted, alkyl groups may be substituted with up to 5 substituent groups, selected from the groups as herein defined, at any available point of attachment. When the alkyl group is said to be substituted with an alkyl group, this is used interchangeably with “branched alkyl group”.
Cycloalkyl is a species of alkyl containing from 3 to 15 carbon atoms, without alternating or resonating double bonds between carbon atoms. It may contain from 1 to 4 rings which are fused. Preferred cycloalkyl groups are cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. When substituted, cycloalkyl groups may be substituted with up to 3 substituents which are defined herein by the definition of alkyl.
The term “alkoxy” refers to those hydrocarbon groups having an oxygen bridge and being in either a straight or branched configuration and if two or more carbon atoms in length, they may include a double or a triple bond. Exemplary of such alkoxy groups are methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, tertiary butoxy, pentoxy, isopentoxy, hexoxy, isohexoxy allyloxy, propargyloxy, and the like.
“Halogen” or “halo” as used herein means fluoro, chloro, bromo and iodo.
The term “alkenyl” refers to a hydrocarbon radical straight, branched or cyclic containing from 2 to 10 carbon atoms and at least one carbon to carbon double bond. Preferred alkenyl groups include ethenyl, propenyl, butenyl and cyclohexenyl. Preferably, alkenyl is C2-C6 alkenyl.
Preferably, alkynyl is C2-C6 alkynyl.
As used herein, “aryl” is intended to mean any stable monocyclic or bicyclic carbon ring of up to 7 members in each ring, wherein at least one ring is aromatic. Examples of such aryl elements include phenyl, naphthyl, tetrahydronaphthyl, indanyl, biphenyl, phenanthryl, anthryl or acenaphthyl.
The term heterocyclyl, heterocycle or heterocyclic, as used herein, represents a stable 5- to 7-membered monocyclic or stable 8- to 11-membered bicyclic heterocyclic ring which is either saturated or unsaturated, and which consists of carbon atoms and from one to four heteroatoms selected from the group consisting of N, O, and S, and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring. The heterocyclic ring may be attached at any heteroatom or carbon atom which results in the creation of a stable structure. The term heterocyclyl, heterocycle or heterocyclic includes heteroaryl moieties. Examples of such heterocyclic elements include, but are not limited to, azepinyl, benzimidazolyl, benzisoxazolyl, benzofurazanyl, benzopyranyl, benzothiopyranyl, benzofuryl, benzothiazolyl, benzothienyl, benzoxazolyl, chromanyl, cinnolinyl, dihydrobenzofuryl, dihydrobenzothienyl, dihydrobenzothiopyranyl, dihydrobenzothiopyranyl sulfone, 1,3-dioxolanyl, furyl, imidazolidinyl, imidazolinyl, imidazolyl, indolinyl, indolyl, isochromanyl, isoindolinyl, isoquinolinyl, isothiazolidinyl, isothiazolyl, isothiazolidinyl, morpholinyl, naphthyridinyl, oxadiazolyl, 2-oxoazepinyl, oxazolyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, piperidyl, piperazinyl, pyridyl, pyrazinyl, pyrazolidinyl, pyrazolyl, pyridazinyl, pyrimidinyl, pyrrolidinyl, pyrrolyl, quinazolinyl, quinolinyl, quinoxalinyl, tetrahydrofuryl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, thiamorpholinyl, thiamorpholinyl sulfoxide, thiazolyl, thiazolinyl, thienofuryl, thienothienyl, and thienyl. An embodiment of the examples of such heterocyclic elements include, but are not limited to, azepinyl, benzimidazolyl, benzisoxazolyl, benzofurazanyl, benzopyranyl, benzothiopyranyl, benzofuryl, benzothiazolyl, benzothienyl, benzoxazolyl, chromanyl, cinnolinyl, dihydrobenzofuryl, dihydrobenzothienyl, dihydrobenzothiopyranyl, dihydrobenzothiopyranyl sulfone, furyl, imidazolidinyl, imidazolinyl, imidazolyl, indolinyl, indolyl, isochromanyl, isoindolinyl, isoquinolinyl, isothiazolidinyl, isothiazolyl, isothiazolidinyl, morpholinyl, naphthyridinyl, oxadiazolyl, 2-oxoazepinyl, oxazolyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, piperidyl, piperazinyl, pyridyl, 2-pyridinonyl, pyrazinyl, pyrazolidinyl, pyrazolyl, pyridazinyl, pyrimidinyl, pyrrolidinyl, pyrrolyl, quinazolinyl, quinolinyl, quinoxalinyl, tetrahydrofuryl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, thiamorpholinyl, thiamorpholinyl sulfoxide, thiazolyl, thiazolinyl, thienofuryl, thienothienyl, thienyl and triazolyl.
Preferably, heterocycle is selected from 2-azepinonyl, benzimidazolyl, 2-diazapinonyl, imidazolyl, 2-imidazolidinonyl, indolyl, isoquinolinyl, morpholinyl, piperidyl, piperazinyl, pyridyl, pyrrolidinyl, 2-piperidinonyl, 2-pyrimidinonyl, 2-pyrollidinonyl, quinolinyl, tetrahydrofuryl, tetrahydroisoquinolinyl, and thienyl.
As used herein, “heteroaryl” is intended to mean any stable monocyclic or bicyclic carbon ring of up to 7 members in each ring, wherein at least one ring is aromatic and wherein from one to four carbon atoms are replaced by heteroatoms selected from the group consisting of N, O, and S. Examples of such heterocyclic elements include, but are not limited to, benzimidazolyl, benzisoxazolyl, benzofurazanyl, benzopyranyl, benzothiopyranyl, benzofuryl, benzothiazolyl, benzothienyl, benzoxazolyl, chromanyl, cinnolinyl, dihydrobenzofuryl, dihydrobenzothienyl, dihydrobenzothiopyranyl, dihydrobenzothiopyranyl sulfone, furyl, imidazolyl, indolinyl, indolyl, isochromanyl, isoindolinyl, isoquinolinyl, isothiazolyl, naphthyridinyl, oxadiazolyl, pyridyl, pyrazinyl, pyrazolyl, pyridazinyl, pyrimidinyl, pyrrolyl, quinazolinyl, quinolinyl, quinoxalinyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, thiazolyl, thienofuryl, thienothienyl, thienyl and triazolyl.
As used herein, unless otherwise specifically defined, substituted alkyl, substituted cycloalkyl, substituted aroyl, substituted aryl, substituted heteroaroyl, substituted heteroaryl, substituted arylsulfonyl, substituted heteroaryl-sulfonyl and substituted heterocycle include moieties containing from 1 to 4 substituents, preferably 1 to 3 substituents in addition to the point of attachment to the rest of the compound. Preferably, such substituents are selected from the group which includes but is not limited to F, Cl, Br, CF3, NH2, N(C1-C6 alkyl)2, NO2, CN, (C1-C6 alkyl)O—, (aryl)O(C1-C6 alkyl)C(O)NH—, H2N—C(NH)—, (C1-C6 alkyl)C(O)—, (C1-C6 alkyl)OC(O)—, (C1-C6 alkyl)OC(O)NH—, phenyl, pyridyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, thienyl, furyl, isothiazolyl, C1-C20 alkyl, (CH2)nOH, CF3, (CH2)nC(O)OH, (CH2)nC(O)OC1-6 alkyl, (CH2)nC(O)NR7R8, (CH2)nC5-10 heterocyclyl, SO2NR5R6, (CH2)C6-10 aryl, N(R)2, NO2, CN, (C1-6 alkyl)O—, (aryl)O—, (C1-6 alkyl)S(O)0-2—, C1-12 alkyl, said heterocyclyl, and aryl optionally substituted with 1 to 3 groups selected from the group consisting of (CH2)nOR, (CH2)nN(R)2, —O—;
When a functional group is termed “protected”, this means that the group is in modified form to preclude undesired side reactions at the protected site. Suitable protecting groups for the compounds of the present invention will be recognized from the present application taking into account the level of skill in the art, and with reference to standard textbooks, such as Greene, T. W. et al. Protective Groups in Organic Synthesis Wiley, New York (1991). Examples of suitable protecting groups are contained throughout the specification.
The compounds of the present invention are basic therefore salts may be prepared from pharmaceutically acceptable non-toxic acids, including inorganic and organic acids. Such acids include acetic, benzenesulfonic, benzoic, camphorsulfonic, citric, ethanesulfonic, fumaric, gluconic, glutamic, hydrobromic, hydrochloric, isethionic, lactic, maleic, malic, mandelic, methanesulfonic, mucic, nitric, pamoic, pantothenic, phosphoric, succinic, sulfuric, tartaric, p-toluenesulfonic acid and the like. Particularly preferred are citric, hydrobromic, hydrochloric, maleic, phosphoric, sulfuric and tartaric acids.
The preparation of the pharmaceutically acceptable salts described above and other typical pharmaceutically acceptable salts is more fully described by Berg et al., “Pharmaceutical Salts,” J. Pharm. Sci., 1977:66:1-19.
An embodiment of this invention is realized when R1 represents —C1-6 alkyl, preferably methyl, and C3-6 cycloalkyl, and all other variables are as described herein.
Another embodiment of this invention is realized when R1 represents H, and all other variables are as described herein.
Another embodiment of this invention is realized when R2 represents OC1-6 alkyl, preferably the alkyl is methyl, and all other variables are as described herein.
Another embodiment of this invention is realized when R2 represents OH and all other variables are as described herein.
Another embodiment of this invention is realized when R2 represents H and all other variables are as described herein.
Another embodiment of this invention is realized when R1 represents H, R2 represents OH and all other variables are as described herein.
Another embodiment of this invention is realized when R3 represents C(O)NR5R6, and all other variables are as described herein.
Another embodiment of this invention is realized when R3 represents —C(O)NHC(R7R8)C(O)NR5R6, and all other variables are as described herein.
Another embodiment of this invention is realized when R1 represents H, R2 represents OH, R3 represents C(O)NR5R6, and all other variables are as described herein. A sub-embodiment of this invention is realized when R3 represents —CONHC(═CH2)C(O)NH2 and all other variables are as described herein.
Another embodiment of this invention is realized when R3 represents —C(O)OR5, and all other variables are as described herein.
Another embodiment of this invention is realized when R4 represents
and all other variables are as described herein. A sub-embodiment of this invention is realized when R represents H, R1 represents H, R2 represents OH, R3 represents C(O)NR5R6, and all other variables are as described herein. A sub-embodiment of this invention is realized when R3 represents —CONHC(═CH2)C(O)NH2 and all other variables are as described herein.
Another embodiment of this invention is realized when R4 represents
and all other variables are as described herein. A sub-embodiment of this invention is realized when R represents H, R1 represents H, R2 represents OH, R3 represents C(O)NR5R6, and all other variables are as described herein. A sub-embodiment of this invention is realized when R3 represents —CONHC(═CH2)C(O)NH2 and all other variables are as described herein.
Another embodiment of this invention is realized when R4 represents
and all other variables are as described herein. A sub-embodiment of this invention is realized when R1 represents H, R2 represents OH, R3 represents C(O)NR5R6, and all other variables are as described herein. A sub-embodiment of this invention is realized when R3 represents —CONHC(═CH2)C(O)NH2 and all other variables are as described herein.
Another embodiment of this invention is realized when R4 represents
and all other variables are as described herein. A sub-embodiment of this invention is realized when R1 represents H, R2 represents OH, R3 represents C(O)NR5R6, and all other variables are as described herein. A sub-embodiment of this invention is realized when R3 represents —CONHC(═CH2)C(O)NH2 and all other variables are as described herein.
Still another embodiment of this invention is realized when R5 and R6 independently represent hydrogen, C1-12 alkyl, —(CH2)nC(═CH2)C(O)NH2, —(CH2)nC(═CH2)CN, —(CH2)nC5-10 heterocyclyl, —(CH2)nNR7R8, —(CH2)nNR(CH2)nNR7R8, —(CH2)nNR(CH2)nC5-10 heterocyclyl, —(CH2)nC6-10 aryl, —(CH2)n(O(CH2)2)1-6R9, —(CH2)nNHC(O)(CH2)nNR7R8, said aryl, and heterocyclyl optionally substituted with one or more groups of Ra; said alkyl optionally substituted with 1 to 6 hydroxy and/or optionally substituted by one or more groups of Ra.
Another embodiment of this invention is realized when one of R5 and R6 is hydrogen and the other is C1-12 alkyl, —(CH2)nC(═CH2)C(O)NH2, —(CH2)nC(═CH2)CN, —(CH2)nC5-10 heterocyclyl, —(CH2)nNR7R8, —(CH2)nNR(CH2)nNR7R8, —(CH2)nNR(CH2)nC5-10 heterocyclyl, —(CH2)nC6-10 aryl, —(CH2)n(O(CH2)2)1-6R9, —(CH2)nNHC(O)(CH2)nNR7R8, said heterocyclyl selected from the group consisting of pyrimidinyl, morpholinyl, piperazinyl, pridinyl, pyrazolyl, indolyl, furanyl, isoindazolyl, pyrazinyl, pyrrolyl, imidazolyl, triazolyl or teterazolyl and optionally substituted with 1 to 3 groups of Ra; said alkyl optionally substituted with 1 to 6 hydroxy and/or optionally substituted by one to three groups of Ra, Still another embodiment of this invention is realized by structural formula II:
wherein R1 R2, R4, and R4a, are as described herein. A sub-embodiment of the invention of formula II is realized when R4 is:
and R4a is C1-12 alkyl, C(O)C1-12 alkyl, —(CH2)nC(O)NR5R6, —(CH2)nNR5R6, —(CH2)nC5-10 heterocylyl, said heterocyclyl optionally substituted with one or more groups of Ra; said alkyl optionally substituted with 1 to 6 hydroxy and/or optionally substituted by one or more groups of Ra. Still another sub-embodiment of this invention is realized when R4a is —(CH2)nC(O)NR5R6, or —(CH2)nNR5R6.
Yet another sub-embodiment of the invention of formula II is realized when R4 is
and R4a is C1-12 alkyl, C(O)C1-12 alkyl, —(CH2)nC(O)NR5R6, —(CH2)nNR5R6, —(CH2)nC5-10 heterocylyl, said heterocyclyl optionally substituted with one or more groups of Ra; said alkyl optionally substituted with 1 to 6 hydroxy and/or optionally substituted by one or more groups of Ra. Still another sub-embodiment of this invention is realized when R4a is —(CH2)nC(O)NR5R6, or —(CH2)nNR5R6.
Another-embodiment of this invention is realized when R3 is —C(O)NH(CH2)nX, wherein X is selected from the group consisting of phenyl, pyrimidinyl, morpholinyl, piperazinyl, pridinyl, pyrazolyl, indolyl, furanyl, isoindazolyl, pyrazinyl, pyrrolyl, imidazolyl, triazolyl and teterazolyl said X groups optionally substituted with 1 to 3 groups of Ra.
Preferred compounds of this invention are found in Table 1 below:
or a pharmaceutically acceptable salt, ester, enantiomer, diasteriomer or mixture thereof.
The compounds of this invention are a broad spectrum antibiotic useful in the treatment of bacterial infections. They demonstrate antibacterial activity primarily against S. aureus, E. faecalis, E. faecium, S. pneumonieae, B. subtilus including species that are resistant to many known antibiotics. The minimum inhibitory concentration (MIC) values range from 0.0001 to less than 200 μg/mL for test strains such as Staphylococuus aureus, Staphylococuus hemolyticus, Streptococcus pyogenes, Streptococcus pneumoniae, and E. feacalis. The compounds of the invention can be formulated in pharmaceutical compositions by combining the compounds with a pharmaceutically acceptable carrier. Examples of such carriers are set forth below.
The compounds may be employed in powder or crystalline form, in liquid solution, or in suspension. They may be administered by a variety of means; those of principal interest include: topically, orally and parenterally by injection (intravenously or intramuscularly).
Compositions for injection, one route of delivery, may be prepared in unit dosage form in ampules, or in multidose containers. The injectable compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, and may contain various formulating agents. Alternatively, the active ingredient may be in powder (lyophillized or non-lyophillized) form for reconstitution at the time of delivery with a suitable vehicle, such as sterile water. In injectable compositions, the carrier is typically comprised of sterile water, saline or another injectable liquid, e.g., peanut oil for intramuscular injections. Also, various buffering agents, preservatives and the like can be included.
Topical applications may be formulated in carriers such as hydrophobic or hydrophilic bases to form ointments, creams, lotions, in aqueous, oleaginous or alcoholic liquids to form paints or in dry diluents to form powders.
Oral compositions may take such forms as tablets, capsules, oral suspensions and oral solutions. The oral compositions may utilize carriers such as conventional formulating agents, and may include sustained release properties as well as rapid delivery forms.
The dosage to be administered depends to a large extent upon the condition and size of the subject being treated, the route and frequency of administration, the sensitivity of the pathogen to the Compound, the virulence of the infection and other factors. Such matters, however, are left to the routine discretion of the physician according to principles of treatment well known in the antibacterial arts.
The compositions for administration to humans per unit dosage, whether liquid or solid, may contain from about 0.01% to as high as about 99% of Compound I, one embodiment of the range being from about 10-60%. The composition will generally contain from about 15 mg to about 2.5 g of Compound I, one embodiment of this range being from about 250 mg to 1000 mg. In parenteral administration, the unit dosage will typically include pure Compound I in sterile water solution or in the form of a soluble powder intended for solution, which can be adjusted to neutral pH and isotonicity.
The invention described herein also includes a method of treating a bacterial infection in a mammal in need of such treatment comprising the administration of the compound of formula I to the mammal in an amount effective to treat the infection.
One embodiment of the methods of administration of a compound of formula I includes oral and parenteral methods, e.g., i.v. infusion, i.v. bolus and i.m. injection.
For adults, about 5-50 mg of a compound of formula I per kg of body weight given one to four times daily is preferred. The preferred dosage is 250 mg to 1000 mg of the antibacterial given one to four times per day. More specifically, for mild infections a dose of about 250 mg two or three times daily is recommended. For moderate infections against highly susceptible gram positive organisms a dose of about 500 mg three or four times daily is recommended. For severe, life-threatening infections against organisms at the upper limits of sensitivity to the antibiotic, a dose of about 1000-2000 mg three to four times daily may be recommended.
For children, a dose of about 5-25 mg/kg of body weight given 2, 3, or 4 times per day is preferred; a dose of 10 mg/kg is typically recommended.
The compounds of the present invention can be prepared according to Schemes 1-3, using appropriate materials, and are further exemplified by the following specific examples. Thiazomycin and its derivatives may be employed as starting materials for the synthesis of compounds of Formula I. The methylene bridge in the sugar residue of thiazomycin derivatives can be removed to generate the amino alcohol intermediate, which can be further manipulated to give compounds of Formula I, as described in Scheme 1. A natural product designated MJ347-81F4-B, for which R1 is H, R2 is OH, R3 is —C(O)NHC(CH2)C(O)NH 2, and R4 is
is a thazomycin derivative that has been previously described (Sasaki, T. et al, J. of Antibiotics 1998, 51, p 713-721). It can also be obtained from thiazomycin (See PCT US200533326 incorporated herein by reference in its entirety) through the chemical removal of the methylene bridge as described in Scheme 1. Alternatively, the methylene bridge in the sugar residue of thiazomycin derivatives may be directly replaced with other activated aldehydes or ketones, such as glyoxylic acid, to give sugar-substituted analogs. The carboxylic analog can be further functionalized as described in Scheme 2. Necleophilic attack on the methylene bridge by a dialkylphosphite may produce phosphonate analogs (scheme 3).
The compounds illustrated in the examples are not, however, to be construed as forming the only genus that is considered as the invention. The following examples further illustrate details for the preparation of compounds of the present invention. Those skilled in the art will readily understand that known variations of the conditions and processes of the following preparative procedures can be used to prepare the compounds of the present invention. All temperatures are in degrees Celsius unless otherwise noted.
wherein:
Q is a residue of a thiazolyl peptide antibiotic represented by:
wherein R1, R2 & R3 are described herein.
To a solution of thiazomycin (see PCT US200533326) (20 mg) in AcOH (1.0 mL) were added hydroxylamine hydrochloride (10 mg) and 3 drops of water. The reaction mixture was stirred at room temperature for 7 hrs. Purification by preparative reverse phase HPLC gave the desired product (15 mg). LCMS [M+H]+: 1423.3;
To a solution of morpholino thiazomycin analog (see PCT US200533326, 130 mg, 0.088 mmol) in 3 mL of glacial acetic acid was added hydroxylamine hydrochloride (92 mg, 1.32 mmol). The reaction mixture was stirred at room temperature for 40 minutes. Purification by preparative reverse phase HPLC produced the desired product as a yellow solid (60 mg, 46% yield). LCMS [M+H]+: 1468.5; 1H NMR (CD3OD, 600 MHz): 8.60 (d, J=9.0 Hz, 1H), 8.55 (s, 1H), 8.43 (s, 1H), 8.41 (s, 1H), 8.16 (s, 1H), 8.12 (d, J=9.0 Hz, 1H), 7.87 (s, 1H), 7.84-7.80 (m, 3H), 7.41 (t, J=7.8 Hz, 1H), 7.20 (d, J=6.6 Hz, 1H), 6.11 (d, J=12.0 Hz, 1H), 5.87 (dd, J=7.2 Hz, 1.8 Hz, 1H), 5.77-5.74 (m, 1H), 5.38-5.35 (m, 1H), 5.07-4.93 (m, 3H), 4.58-4.56 (m, 1H), 4.42-4.41 (m, 1H), 4.37-4.34 (m, 1H), 4.28 (d, J=10.8 Hz, 1H), 4.06-4.01 (m, 2H), 3.93 (s, 3H), 3.84 (broad s, 3H), 3.46-3.44 (m, 4H), 2.76 (s, 1H), 2.74 (s, 3H), 2.10-2.07 (m, 2H), 2.04 (s, 3H), 1.96-1.92 (m, 3H), 1.86-1.82 (m, 1H), 1.70 (s, 3H), 1.439 (d, J=5.4 Hz, 3H), 0.82 (d, J=6.0 Hz, 3H).
A suspension of Noca-IV (310 mg, 0.23 mmol) and hydroxylamine hydrochloride (236 mg, 3.4 mmol) in 4 mL of acetic acid was stirred at room temperature for 14 hours. Purification by preparative reverse phase HPLC produced the desired product (210 mg, 67% yield) as a yellow powder. LCMS [M+H]+: 1354.2; 1H NMR (CD3OD, 600 MHz): 8.60 (d, J=9.6 Hz, 1H), 8.53 (s, 1H), 8.40 (s, 1H), 8.35 (s, 1H), 8.16 (s, 1H), 8.11 (d, J=10.8 Hz, 1H), 7.82-7.79 (m, 3H), 7.40 (t, J=7.8 Hz, 1H), 7.19 (d, J=6.6 Hz, 1H), 6.10 (d, J=12.0 Hz, 1H), 5.88-5.86 (m, 1H), 5.77-5.74 (m, 1H), 5.37-5.35 (m, 1H), 5.06-5.02 (m, 2H), 4.93 (d, J=10.2 Hz, 1H), 4.57 (d, J=11.4 Hz, 1H), 4.41 (d, J=9.6 Hz, 1H), 4.33 (d, J=4.2 Hz, 1H), 4.05-4.00 (m, 2H), 3.93 (s, 3H), 3.92 (m, 1H), 2.87 (m, 1
A solution of Intermediate 1 (50 mg, 0.035 mmol) and glyoxylic acid (50% in water, 0.2 mL) in 1 mL of DMF was stirred at room temperature for 12 hours. Direct purification by preparative reverse phase HPLC give the desired carboxylic acid as a yellow solid (32 mg, 62% yield). MS [M+H]+: 1478.3.
The product of Example 1 (5 mg, 0.0034 mmol) was mixed with D-glucamine (1.3 mg, 0.0069 mmol) and HOAt (0.5 M in DMF, 14 μL, 0.0069 mmol) in DMF (1 mL). The solution was stirred at room temperature for 20 minutes before PyBop (2 mg, 0.0041 mmol) was introduced. The reaction mixture was stirred at room temperature for another 1 hour. Purification by preparative reverse phase HPLC gave the desired product as a yellow solid (1.3 mg, 26% yield). LCMS [M+H]+: 1642.8; 1H NMR (CD3OD, 600 MHz): 8.72 (s, 1H), 8.57 (m, 1H), 8.52 (d, J=9.6 Hz, 1H), 8.38 (s, 1H), 8.33 (s, 1H), 8.13 (d, J=10.8 Hz, 1H), 8.07 (s, 1H), 7.84-7.78 (m, 4H), 7.72 (m, 4H), 7.38 (t, J=7.8 Hz, 1H), 7.21 (d, J=6.6 Hz, 1H), 6.55 (s, 1H), 6.00-5.98 (m, 2H), 5.78 (s, 1H), 5.73-5.70 (m, 1H), 5.34-5.31 (m, 1H), 5.19-5.09 (m, 2H), 4.88 (d, J=10.2 Hz, 1H), 4.55-4.51 (m, 2H), 4.21 (s, 1H), 4.20 (m, 1H), 3.91 (m, 1H), 3.89 (s, 3H), 3.77-3.71 (m, 2H), 3.68-3.62 (m, 3H), 3.59-3.56 (m, 1H), 3.55-3.53 (m, 1H), 3.46-3.43 (m, 1H), 3.20 (m, 1H), 2.77-2.73 (m, 1H), 2.52 (s, 1H), 2.49 (s, 3H), 2.38-2.35 (m, 1H), 2.02 (s, 3H), 1.85-1.82 (m, 1H), 1.41 (d, J=6.0 Hz, 3H), 1.30 (s, 3H), 0.61 (d, J=6.0 Hz, 3H).
A solution of Intermediate 2 (15 mg, 0.01 mmol) and glyoxylic acid (50% in water, 0.1 mL) in 1 mL of DMF was stirred at room temperature for 12 hours. Purification by preparativer reverse phase HPLC gave the carboxylic acid product as a yellow solid (8 mg). MS [M+H]+: 1523.3
To a solution of the above obtained product (4 mg, 0.0026 mmol) in DMF (1 mL) were added 4-(2-aminoethyl)morpholine (0.9 mg, 0.0066 mmol) and HOAt (0.5 M in DMF, 13 μL, 0.0066 mmol). The reaction mixture was stirred at room temperature for 10 minutes before PyBop (1.1 mg, 0.0021 mmol) was added. The reaction was continued at room temperature for another 2 hour, then purified by preparative reverse phase HPLC to give the desired product as a yellow solid (1.5 mg, 10% yield over 2 steps). LCMS [M+H]+: 1636.9; 1H NMR (CD3OD, 600 MHz): 8.57 (s, 1H), 8.54 (d, J=9.6 Hz, 1H), 8.44 (s, 1H), 8.41 (s, 1H), 8.15 (d, J=10.8 Hz, 1H), 8.14 (s, 1H), 7.87-7.79 (m, 4H), 7.41 (t, J=7.8 Hz, 1H), 7.20 (d, J=6.6 Hz, 1H), 6.08 (d, J=12.0 Hz, 1H), 6.00-5.97 (m, 2H), 5.77-5.74 (m, 1H), 5.37-5.35 (m, 1H), 5.08-5.06 (m, 2H), 4.91 (d, J=10.2 Hz, 1H), 4.58-4.56 (m, 1H), 4.48-4.47 (m, 1H), 4.33-4.28 (m, 4H), 4.01-3.99 (m, 1H), 3.94 (m, 1H), 3.93 (s, 3H), 3.87 (d, J=3.0 Hz, 1H), 3.83 (m, 3H), 3.76-3.75 (m, 2H), 3.45-3.40 (m, 3H), 3.17-3.13 (m, 2H), 2.71 (m, 1H), 2.54 (s, 1H), 2.52 (s, 3H), 2.02 (s, 3H), 1.97-1.95 (m, 2H), 1.90-1.84 (m, 2H), 1.41 (d, J=6.0 Hz, 3H), 1.32 (s, 3H), 0.65 (d, J=6.0 Hz, 3H).
A solution of Intermediate 3 (14 mg, 0.01 mmol) and 2-methyl-2-morpholinopropanal (24 mg, 0.15 mmol) in 1 mL of DMF was stirred at room temperature for 14 hours. Purification by preparative reverse phase HPLC gave the desired product (8 mg, 27% yield) as a yellow powder. LCMS [M+H]+: 1494.0; 1H NMR (CD3OD, 600 MHz): 8.56 (d, J=9.6 Hz, 1H), 8.54 (s, 1H), 8.42 (s, 1H), 8.36 (s, 1H), 8.17 (d, J=10.8 Hz, 1H), 8.14 (s, 1H), 7.86-7.79 (m, 3H), 7.39 (t, J=7.8 Hz, 1H), 7.16 (d, J=6.6 Hz, 1H), 6.04 (d, J=12.0 Hz, 1H), 6.02-6.00 (m, 1H), 5.80-5.77 (m, 1H), 5.38-5.36 (m, 1H), 5.10 (m, 2H), 4.98 (d, J=10.2 Hz, 1H), 4.90 (d, J=11.4 Hz, 1H), 4.57 (d, J=9.6 Hz, 1H), 4.48 (d, J=4.2 Hz, 1H), 4.37 (s, 1H), 4.33 (m, 1H), 4.24 (d, J=10.2 Hz, 1H), 4.00 (m, 1H), 3.92 (s, 3H), 3.91 (m, 1H), 3.72 m, 2H), 3.58 (m, 1H), 3.48 (m, 1H), 2.80 (m, 1H), 2.78 (m, 1H), 2.53 (s, 3H), 2.48-2.46 (m, 1H), 2.02 (s, 3H), 1.91-1.87 (m, 1H), 1.41-1.34 (m, 10H), 0.63 (d, J=6.0 Hz, 3H).
A solution of Intermediate 3 (14 mg, 0.01 mmol) and 6-morphilin-4-yl-pyridine-3-carbaldehyde (30 mg, 0.15 mmol) in 1 mL of DMF was stirred at room temperature for 14 hours. Purification by preparative reverse phase HPLC gave the desired product (8 mg, 27% yield) as a yellow powder. LCMS [M+H]+: 1529.0; 1H NMR (CD3OD, 600 MHz): 8.65 (s, 1H), 8.52 (d, J=9.6 Hz, 1H), 8.39 (s, 1H), 8.35 (s, 1H), 8.15 (d, J=10.8 Hz, 1H), 8.12 (s, 1H), 8.04 (s, 1H), 7.85 (m, 1H), 7.81-7.79 (m, 3H), 7.40 (t, J=7.8 Hz, 1H), 7.16 (d, J=6.6 Hz, 1H), 6.04-6.01 (m, 2H), 5.77 (m, 1H), 5.36 (m, 1H), 5.07-5.01 (m, 3H), 4.98 (d, J=10.2 Hz, 1H), 4.90 (d, J=11.4 Hz, 1H), 4.56-4.52 (m, 2H), 4.32 (m, 1H), 4.23 (m, 1H), 3.96 (d, J=10.2 Hz, 1H), 3.91 (s, 3H), 3.82-3.81 (m, 3H), 3.62-3.60 (m, 3H), 2.80 (m, 2H), 2.44 (m, 3H), 2.01 (s, 3H), 1.94-1.89 (m, 1H), 1.42 (m, 6H), 0.70 (d, J=6.0 Hz, 3H).
A solution of Intermediate 1 (5 mg, 0.0035 mmol) and betaine aldehyde chloride (5 mg, 0.035 mmol) in 0.5 mL of DMF was stirred at room temperature for 24 hours. Purification by preparative reverse phase HPLC gave the desired product (1.2 mg, 23% yield) as a yellow powder. LCMS [M]+: 1506.8; 1H NMR (CD3OD, 600 MHz): 8.56 (s, 1H), 8.52 (d, J=9.6 Hz, 1H), 8.48 (s, 1H), 8.41 (s, 1H), 8.17 (s, 2H), 8.15 (s, 1H), 7.87 (s, 1H), 7.83 (m, 1H), 7.80 (m, 2H), 7.40 (t, J=7.8 Hz, 1H), 7.19 (d, J=6.6 Hz, 1H), 6.05-6.02 (m, 2H), 5.77-5.75 (m, 1H), 5.38-5.36 (m, 1H), 5.25-5.20 (m, 1H), 5.06-5.02 (m, 2H), 4.93 (d, J=10.8 Hz, 1H), 4.56 (d, J=11.4 Hz, 1H), 4.51 (d, J=9.6 Hz, 1H), 4.48 (d, J=6.0 Hz, 1H), 4.33 (broad s, 1H), 4.27 (d, J=10.8 Hz, 1H), 4.20 (broad s, 1H), 4.04 (s, 9H), 3.93 (s, 3H), 3.84 (m, 1H), 3.66-3.60 (m, 2H), 3.41 (s, 1H), 3.09 (s, 3H), 2.93 (broad s, 3H), 2.81 (broad s, 1H), 2.64 (s, 1H), 2.46 (m, 1H), 2.03 (s, 3H), 2.01-1.97 (m, 1H), 1.91 (s, 1H), 1.52 (s, 3H), 1.40 (broad s, 3H), 1.29 (m, 2H), 0.87 (d, J=6.6 Hz, 3H).
A solution of Intermediate 1 (5 mg, 0.0035 mmol) and D-ribose (5 mg, 0.035 mmol) in 0.5 mL of DMF was stirred at room temperature for 24 hours. Purification by preparative reverse phase HPLC gave the desired product (1.1 mg, 20% yield) as a yellow powder. LCMS [M+H]+: 1539.3; 1H NMR (CD3OD, 600 MHz): 8.68 (s, 1H), 8.61 (d, J=9.6 Hz, 1H), 8.43-8.42 (m, 2H), 8.18-8.13 (m, 2H), 7.86 (m, 2H), 7.77 (m, 2H), 7.41 (t, J=7.8 Hz, 1H), 7.20 (d, J=6.6 Hz, 1H), 6.56 (s, 1H), 6.10 (d, J=12.0 Hz, 1H), 5.87 (d, J=11.4 Hz, 1H), 5.82 (s, 1H), 5.76-5.75 (m, 1H), 5.35-5.34 (m, 1H), 5.07 (d, J=10.2 Hz, 1H), 5.03 (d, J=11.4 Hz, 1H), 4.92 (d, J=12.0 Hz, 1H), 4.55-4.53 (m, 2H), 4.40 (m, 1H), 4.28 (m, 1H), 4.17 (m, 1H), 4.05-4.03 (m, 2H), 3.96 (m, 1H), 3.92 (s, 3H), 2.94 (s, 1H), 2.77 (s, 3H), 2.10 (m, 1H), 2.06 (s, 3H), 1.87-1.85 (m, 1H), 1.72 (s, 3H), 1.39 (Broad s, 3H), 0.84 (d, J=6.0 Hz, 3H).
To a solution of Intermediate 1 (15 mg) and 1,4-dioxane-2,5-diol (2.4 mg, 2 eq.) in anhydrous DMF (0.2 mL) was added NaBH4 (4 eq.) portion-wise at room temperature. The reaction was stirred for 15 min and quenched by water. The reaction mixture was acidified by adding TFA and was directly purified by preparative reverse phase HPLC. The pure fractions were collected and lyophilized to afford TFA salt of the desired product. LCMS [M+H]+: 1467.8; 1H NMR (600 MHz, CD3OD) δ 8.62 (d, J=9.0 Hz, 1H), 8.49 (s, 1H), 8.45 (s, 1H), 8.40 (s, 1H), 8.15 (s, 1H), 8.01 (m, 1H), 7.96 (d, J=11.4 Hz, 1H), 7.77 (m, 1H), 7.72 (d, J=8.4 Hz, 1H), 7.56 (d, J=7.2 Hz, 1H), 7.42 (t, J=7.2, 1H), 7.24 (d, J=6.6 Hz, 1H), 6.43 (s, 1H), 6.11 (d, J=6.6 Hz, 1H), 5.88 (dd, J=8.0, 1.8 Hz, 1H), 5.85 (dd, J=10.8, 4.8 Hz, 1H), 5.75 (s, 1H), 5.47 (d, J=8.0 Hz, 1H), 5.18 (s, 1H), 5.04 (d, J=12.6 Hz, 1H), 4.99 (d, J=10.8 Hz, 1H), 4.56 (s, 1H), 4.50 (d, J=10.2 Hz, 1H), 4.41 (m, 1H), 4.18 (d, J=10.2 Hz, 1H), 4.09 (d, J=6.0, 1H), 4.06 (d, J=8.0 Hz, 1H), 3.95 (s, 3H), 3.90 (t, J=6.6 Hz, 2H), 3.46 (m, 1H), 3.41 (s, 1H), 3.17 (s, 1H), 3.12 (m, 1), 2.97 (s, 6H), 2.64 (s, 1H), 2.14 (s, 2H), 2.08 (s, 3H), 1.97 (s, 2H), 1.94 (d, J=6.6 Hz, 3H), 1.70 (s, 2H), 1.32 (s, 3H), 1.22 (d, J=5.4 Hz, 3H), 0.95 (d, J=6.0 Hz, 3H).
A solution of thiazomycin (3 mg) in neat diethylphosphite (0.5 mL) was heated at 50° C. for 7 hrs. Purification by reverse phase HPLC gave the desired product (1.0 mg). LCMS [M+H]+: 1573.3; 1H NMR (CD3OD, 600 MHz): 8.66 (s, 1H), 8.60 (s, 1H), 8.59 (d, J=9.4 Hz, 1H), 8.43 (s, 1H), 8.37 (s, 1H), 8.17 (d, J=11 Hz, 1H), 8.12 (s, 1H), 7.9-7.8 (m, 3H), 7.44 (t, J=7.5 Hz, 1H), 7.22 (d, J=7.1 Hz, 1H), 6.58 (s, 1H), 6.13 (d, J=12.6 Hz, 1H), 5.88 (d, J=9.4 Hz, 1H), 5.81 (s, 1H), 5.75 (m, 1H), 5.37 (m, 1H), 5.08 (d, J=4.6 Hz, 1H), 5.04 (d, J=12.8 Hz, 1H), 4.95 (d, J=10.5 Hz, 1H), 4.55 (d, J=10.4 Hz, 1H), 4.41 (d, J=9.8 Hz, 1H), 4.32-4.43 (m, 2H), 4.2-4.1 (m, 4H), 4.02 (m, 2H), 3.94 (m, 1H), 3.93 (s, 3H), 3.78 (m, 1H), 3.20 (m, 1H), 2.80 (s, 3H), 2.79 (m, 1H), 2.50 (m, 1H), 2.13 (m, 1H), 2.05 (s, 3H), 2.04 (m, 1H), 1.62 (s, 3H), 1.43 (d, J=6.0 Hz, 3H), 1.36 (t, J=7.1 Hz, 6H), 0.81 (d, J=6.6 Hz, 3H).
The antibacterial activity of the compounds of Formula I can be determined using the assay methods described below.
50% Lysed Horse Blood (LHB; BBL) (stored frozen)
Trypticase Soy Broth (TSB, 5 mL/tube; BBL)
MIC 2000 Microtiter plate inoculator.
2× Trypticase Soy Broth (TSB, BBL)+15% glycerol/50% horse serum.
96-Well Microtiter plates, lids, inoculum trays (Dynex Laboratories)
8-Channel Finn Multichannel pipettor, 0.5-10 μL volume
Cation-Adjusted Mueller Hinton Broth (BBL): Prepared according to manufacturer's instructions (22 gms dissolved in 1000 mL water; autoclaved 22 minutes). Stored refrigerated. Filter-sterilized before use using a Corning 0.45 ™ cellulose acetate filter.
50% Lysed Horse Blood: Defibrinated horse blood is diluted 1:1 with sterile distilled water; frozen, thawed and re-frozen (at least 7 times), then centrifuged. Stored frozen at −20° C.
Cation-Adjusted Mueller Hinton+2.5% Lysed Horse Blood: Aseptically add 5 mL 50% lysed horse blood to 100 mL Cation-Adjusted Mueller Hinton Broth. Filter-sterilize before use using a Corning 0.45 ™ cellulose acetate filter.
Cation-Adjusted Mueller Hinton+50% Human Serum: Aseptically add 50 mL Human Serum to 50 mL 2× Cation-Adjusted Mueller Hinton Broth. Filter-sterilize before use using a Corning 0.45 Tm cellulose acetate filter.
Haemophilus Test Medium (Remel): Received prepared from manufacturer. Filter-sterilized before use using a Corning 0.45 Tm cellulose acetate filter.
0.9% Sodium Chloride (Saline; Abbott Labs): Received prepared from manufacturer.
2× Skim Milk (Remel): Received prepared from manufacturer.
All agar plates are received prepared from manufacturer.
BACILLUS,
STAPHYLOCOCCUS,
ENTEROCOCCUS:
ESCHERICHI:,
STREP. PNEUMONIAE:
HAEMOPHILUS
INFLUENZAE:
CANDIDA:
The type of strains listed above can be obtained from publicly available sources. The strain of Haemophilus influenzae used in to assay the compound of this invention is a mouse pathogen used for in vivo testing at Merck. The Escherichia coli strain used in to assay the compound of this invention is a cell wall permeable strain. The Candida albicans strain is used as a control. These culture are maintained as frozen stocks at −80° C. in a) Microbank beads; b) 2× Skim Milk; or c) in 2× Trypticase Soy Broth+15% glycerol/50% horse serum (Haemophilus and Streptococcus pneumoniae).
Selected isolates are sub-cultured onto either Chocolate Agar Plates (Haemophilus influenzae), onto Trypticase Soy+5% Sheep Blood Agar Plates (Streptococcus pneumoniae, Staphylococcus aureus, Escherichia coli, Enterococcus, Bacillus) or onto Sabouraud Dextrose Agar (Candida) and incubated at 35° C. Haemophilus and Streptococcus pneumoniae are incubated in 5% CO2; all other isolates are incubated in ambient air. Isolates are sub-cultured 2× before assay.
Colonies are selected from plates and used to prepare an inoculum equivalent to a 0.5 McFarland standard in Trypticase Soy Broth. An inoculum with a density equivalent to a 1.0 McFarland standard is prepared for Streptococcus pneumoniae. The inoculum density for all cultures is ˜108 CFU/mL in TSB. This TSB inoculum is diluted 1:10 in sterile saline (4 mL inoculum+36 mL saline; equivalent to ˜107 CFU/mL) and kept on ice until used to inoculate microtiter plates.
Colony counts are performed on randomly-selected isolates to confirm CFU/well (TSB inoculum plated out 10−5, 10−6 onto either TSA II+5% SB or onto chocolate agar plates, incubated overnight, 35° C., CO2)
All wells of 96-well microtiter plates (Dynex) are filled with 100 TL media. Haemophilus test media plates are prepared to test Haemophilus influenzae; Cation-Adjusted Mueller Hinton+5% Lysed Horse Blood plates are prepared to test Streptococcus pneumoniae; Cation-Adjusted Mueller Hinton Broth plates are prepared to test Enterococcus, Staphylococcus aureus, Escherichia coli and Bacillus subtilis. RPMI 1640 is used to test Candida. The MICs against S. aureus Smith are determined in Cation-adjusted Mueller Hinton and in Cation-Adjusted Mueller Hinton+50% Human Serum, to determine if the compound is inactivated by some component in serum (indicated by an increase in the MIC). Filled plates are wrapped in plastic bags (to minimize evaporation), stored frozen and thawed before use.
The compounds are prepared on a weight basis. Compounds are prepared to 2-10 mg/mL in 100% DMSO, then diluted to 1 mg/mL in a 1:1 dilution of DMSO/2×CAMHB (final concentration=50% DMSO/50% CAMHB). Compounds are serially diluted 1:1 in 50% DMSO/50% CAMHB in BD Biosciences Deep Well Polypropylene 96 well plates (starting concentration 1-5 mg/mL).
Using a Finn Automated Multichannel Pipette, (0.5-10 μL volume) 6.4 TLs of antimicrobial working solutions are added to wells of filled microtiter plates (concentration of antimicrobial in first well=512-64 microg/mL; concentration of DMSO=3.2%). Antimicrobials are added in this manner to keep constant the amount of DMSO in each well (to keep compounds solubilized and to account for the possibility of non-specific killing by the DMSO. The last row contains a growth control of 3.2% DMSO.
Controls (Penicillin G and chloramphenicol) are run with each assay. The controls are prepared in the same manner as described for the compounds of the invention. Ertapenem is included as a control for the serum protein binding assay.
All wells of microtiter plates are inoculated with (saline-diluted) culture using the MIC 2000 System, an automated plate inoculating device which delivers an inoculum of 1.5 TL per well. Plates are incubated at 35° C. in ambient air. An uninoculated plate is also incubated as a sterility check. Results are recorded after 22-24-hours' incubation. Plates were read to no growth. The MIC is defined as the lowest antimicrobial level which resulted in no growth after 22-24-hours' incubation.
The Compounds of formula I demonstrate antibacterial activity against various strains of S. aureus, E. faecalis, E. faecium, B. subtilis and S. pneumoniae. Compounds of formula I also demonstrate antibacterial activity against various species that are resistant to many known antibiotics such as methicillin-resistant S. aureus (MRSA), vancomycin-resistant Enterococcus sp. (VRE), multidrug-resistant E. faecium, macrolide-resistant S. aureus and S. epidermidis, and linezolid-resistant S. aureus and E. faecium. The minimum inhibitory concentration (MIC) values for these test strains range from 0.0001 to 200 μg/mL. MICs are obtained in accordance to the NCCLS guidelines. Select compounds of this invention have been found to have minimum inhibitory concentration (MIC) values that are at least a 10 fold improvement over the compounds disclosed in P. Hrnciar, et. al., J. Org. Chem. 2002, 67, 8789-8793 against tested strains. See Table 2 where compounds A and B (Examples 3 and 10 of claimed invention) were compared with compound C (example 7 of J. Org. Chem. 2002, 67, 8789-8793).
Enterococcus Faecalia
Staphylococcus Aureus
Staphylococcus Aureus
Staphylococcus Aureus
Enterococcus Faecalia
Staphylococcus Aureus
Staphylococcus Aureus
Staphylococcus Aureus
Enterococcus Faecalia
Staphylococcus Aureus
Staphylococcus Aureus
Staphylococcus Aureus
| Number | Date | Country | |
|---|---|---|---|
| 60853340 | Oct 2006 | US |
