ZA200105066B - Alkynyl containing hydroxamic acid compounds as TACE inhibitors. - Google Patents
Alkynyl containing hydroxamic acid compounds as TACE inhibitors. Download PDFInfo
- Publication number
- ZA200105066B ZA200105066B ZA200105066A ZA200105066A ZA200105066B ZA 200105066 B ZA200105066 B ZA 200105066B ZA 200105066 A ZA200105066 A ZA 200105066A ZA 200105066 A ZA200105066 A ZA 200105066A ZA 200105066 B ZA200105066 B ZA 200105066B
- Authority
- ZA
- South Africa
- Prior art keywords
- ynyloxy
- phenyl
- butynyloxy
- hydroxy
- carbon atoms
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims description 32
- 125000000304 alkynyl group Chemical group 0.000 title claims description 7
- 239000002253 acid Substances 0.000 title claims description 6
- NEAQRZUHTPSBBM-UHFFFAOYSA-N 2-hydroxy-3,3-dimethyl-7-nitro-4h-isoquinolin-1-one Chemical compound C1=C([N+]([O-])=O)C=C2C(=O)N(O)C(C)(C)CC2=C1 NEAQRZUHTPSBBM-UHFFFAOYSA-N 0.000 title description 5
- 239000002447 tumor necrosis factor alpha converting enzyme inhibitor Substances 0.000 title description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 48
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 31
- 229910052739 hydrogen Inorganic materials 0.000 claims description 24
- 239000001257 hydrogen Substances 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 125000003118 aryl group Chemical group 0.000 claims description 19
- 125000005842 heteroatom Chemical group 0.000 claims description 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 15
- 229910052717 sulfur Inorganic materials 0.000 claims description 15
- 229910052760 oxygen Inorganic materials 0.000 claims description 14
- 108060008682 Tumor Necrosis Factor Proteins 0.000 claims description 9
- 102100040247 Tumor necrosis factor Human genes 0.000 claims description 9
- ZXKINMCYCKHYFR-UHFFFAOYSA-N aminooxidanide Chemical compound [O-]N ZXKINMCYCKHYFR-UHFFFAOYSA-N 0.000 claims description 9
- 125000001072 heteroaryl group Chemical group 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 102000004190 Enzymes Human genes 0.000 claims description 7
- 108090000790 Enzymes Proteins 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 6
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims description 5
- XAAKCCMYRKZRAK-UHFFFAOYSA-N isoquinoline-1-carboxylic acid Chemical compound C1=CC=C2C(C(=O)O)=NC=CC2=C1 XAAKCCMYRKZRAK-UHFFFAOYSA-N 0.000 claims description 5
- 230000001404 mediated effect Effects 0.000 claims description 5
- 206010039073 rheumatoid arthritis Diseases 0.000 claims description 5
- 208000031886 HIV Infections Diseases 0.000 claims description 4
- 208000037357 HIV infectious disease Diseases 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 206010061218 Inflammation Diseases 0.000 claims description 4
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims description 4
- 206010022489 Insulin Resistance Diseases 0.000 claims description 4
- 208000033519 human immunodeficiency virus infectious disease Diseases 0.000 claims description 4
- 230000004054 inflammatory process Effects 0.000 claims description 4
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 4
- 206010006895 Cachexia Diseases 0.000 claims description 3
- 208000028257 Joubert syndrome with oculorenal defect Diseases 0.000 claims description 3
- 206010040070 Septic Shock Diseases 0.000 claims description 3
- 206010052779 Transplant rejections Diseases 0.000 claims description 3
- VSBFNCXKYIEYIS-UHFFFAOYSA-N Xanthene-9-carboxylic acid Chemical compound C1=CC=C2C(C(=O)O)C3=CC=CC=C3OC2=C1 VSBFNCXKYIEYIS-UHFFFAOYSA-N 0.000 claims description 3
- 125000001589 carboacyl group Chemical group 0.000 claims description 3
- 210000003169 central nervous system Anatomy 0.000 claims description 3
- 125000004475 heteroaralkyl group Chemical group 0.000 claims description 3
- 208000027866 inflammatory disease Diseases 0.000 claims description 3
- 230000002401 inhibitory effect Effects 0.000 claims description 3
- 230000036303 septic shock Effects 0.000 claims description 3
- ZFKRMQURYQDVLG-UHFFFAOYSA-N 2-(2-but-2-ynoxyphenyl)sulfonyloctanoic acid Chemical compound CCCCCCC(C(O)=O)S(=O)(=O)C1=CC=CC=C1OCC#CC ZFKRMQURYQDVLG-UHFFFAOYSA-N 0.000 claims description 2
- SETFXJLLFMSYRI-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenoxy)-n-hydroxyacetamide Chemical compound CC#CCOC1=CC=C(OCC(=O)NO)C=C1 SETFXJLLFMSYRI-UHFFFAOYSA-N 0.000 claims description 2
- WJPUEGIRFDUQBD-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-6-[(2,2-diphenylacetyl)amino]-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)CCCCNC(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 WJPUEGIRFDUQBD-UHFFFAOYSA-N 0.000 claims description 2
- GWGMYUDABVIUOE-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-6-[[2-(3,4-dichlorophenyl)acetyl]amino]-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)CCCCNC(=O)CC1=CC=C(Cl)C(Cl)=C1 GWGMYUDABVIUOE-UHFFFAOYSA-N 0.000 claims description 2
- BIBRWOGPAHSTEO-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-6-[[2-[(2,2-diphenylacetyl)amino]acetyl]amino]-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)CCCCNC(=O)CNC(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 BIBRWOGPAHSTEO-UHFFFAOYSA-N 0.000 claims description 2
- NINCQSFEKDZCJG-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-n-hydroxy-6-(4-thiophen-2-ylbutanoylamino)hexanamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)CCCCNC(=O)CCCC1=CC=CS1 NINCQSFEKDZCJG-UHFFFAOYSA-N 0.000 claims description 2
- XTAJRMPBIDLCQT-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-n-hydroxypropanamide Chemical compound CC#CCOC1=CC=C(SC(C)C(=O)NO)C=C1 XTAJRMPBIDLCQT-UHFFFAOYSA-N 0.000 claims description 2
- RUHRTHITUPDKIR-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfinyl-6-[(2,2-diphenylacetyl)amino]-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)C(C(=O)NO)CCCCNC(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 RUHRTHITUPDKIR-UHFFFAOYSA-N 0.000 claims description 2
- YOUSGMDITBYJFB-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfinyl-6-[[2-(1,3-dioxoisoindol-2-yl)acetyl]amino]-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)C(C(=O)NO)CCCCNC(=O)CN1C(=O)C2=CC=CC=C2C1=O YOUSGMDITBYJFB-UHFFFAOYSA-N 0.000 claims description 2
- BMLZCPWNCNXXRV-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfinyl-n-hydroxy-6-[[2-(1h-indol-3-yl)acetyl]amino]hexanamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)C(C(=O)NO)CCCCNC(=O)CC1=CNC2=CC=CC=C12 BMLZCPWNCNXXRV-UHFFFAOYSA-N 0.000 claims description 2
- JMXDTUHQKRUADR-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfonyl-6-[(2,2-diphenylacetyl)amino]-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)(=O)C(C(=O)NO)CCCCNC(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 JMXDTUHQKRUADR-UHFFFAOYSA-N 0.000 claims description 2
- QRQJWSDLCVXEKN-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfonyl-6-[[2-(1,3-dioxoisoindol-2-yl)acetyl]amino]-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)(=O)C(C(=O)NO)CCCCNC(=O)CN1C(=O)C2=CC=CC=C2C1=O QRQJWSDLCVXEKN-UHFFFAOYSA-N 0.000 claims description 2
- QDUZWZAGLARFAU-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfonyl-6-[[2-(3,4-dichlorophenyl)acetyl]amino]-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)(=O)C(C(=O)NO)CCCCNC(=O)CC1=CC=C(Cl)C(Cl)=C1 QDUZWZAGLARFAU-UHFFFAOYSA-N 0.000 claims description 2
- OQZJOXZSOHZXBH-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfonyl-n-hydroxy-2-methyl-3-(4-phenylphenyl)propanamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)(=O)C(C)(C(=O)NO)CC1=CC=C(C=2C=CC=CC=2)C=C1 OQZJOXZSOHZXBH-UHFFFAOYSA-N 0.000 claims description 2
- FYABASQKYDJSQF-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfonyl-n-hydroxy-2-methyl-3-pyridin-3-ylpropanamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)(=O)C(C)(C(=O)NO)CC1=CC=CN=C1 FYABASQKYDJSQF-UHFFFAOYSA-N 0.000 claims description 2
- CCJYXELKVLVIGZ-UHFFFAOYSA-N 6-[[2-(1-benzothiophen-3-yl)acetyl]amino]-2-(4-but-2-ynoxyphenyl)sulfanyl-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)CCCCNC(=O)CC1=CSC2=CC=CC=C12 CCJYXELKVLVIGZ-UHFFFAOYSA-N 0.000 claims description 2
- RZVCPIHJYJCASG-UHFFFAOYSA-N 6-[[2-(1-benzothiophen-3-yl)acetyl]amino]-2-(4-but-2-ynoxyphenyl)sulfinyl-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)C(C(=O)NO)CCCCNC(=O)CC1=CSC2=CC=CC=C12 RZVCPIHJYJCASG-UHFFFAOYSA-N 0.000 claims description 2
- KSVVUXNDRCMEIH-UHFFFAOYSA-N 6-[[2-(1-benzothiophen-3-yl)acetyl]amino]-2-(4-but-2-ynoxyphenyl)sulfonyl-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)(=O)C(C(=O)NO)CCCCNC(=O)CC1=CSC2=CC=CC=C12 KSVVUXNDRCMEIH-UHFFFAOYSA-N 0.000 claims description 2
- YFECSILBCHJILS-UHFFFAOYSA-N C(C#CC)OC1=CC=C(C=C1)SC(CCCCNC(=O)C=1C=NC2=CC=CC=C2C=1)(O)C(N)=O Chemical compound C(C#CC)OC1=CC=C(C=C1)SC(CCCCNC(=O)C=1C=NC2=CC=CC=C2C=1)(O)C(N)=O YFECSILBCHJILS-UHFFFAOYSA-N 0.000 claims description 2
- ZTUVJKFRGSXMOP-UHFFFAOYSA-N N-[6-amino-5-(4-but-2-ynoxyphenyl)sulfanyl-5-hydroxy-6-oxohexyl]quinoline-2-carboxamide Chemical compound C(C#CC)OC1=CC=C(C=C1)SC(CCCCNC(=O)C1=NC2=CC=CC=C2C=C1)(O)C(N)=O ZTUVJKFRGSXMOP-UHFFFAOYSA-N 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims description 2
- AFDWOSHMSGYFOO-UHFFFAOYSA-N n-[2-[[5-(4-but-2-ynoxyphenyl)sulfanyl-6-(hydroxyamino)-6-oxohexyl]amino]-2-oxoethyl]-2-(2-phenylethyl)benzamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)CCCCNC(=O)CNC(=O)C1=CC=CC=C1CCC1=CC=CC=C1 AFDWOSHMSGYFOO-UHFFFAOYSA-N 0.000 claims description 2
- XTNMCWBPNJENRM-UHFFFAOYSA-N n-[2-[[5-(4-but-2-ynoxyphenyl)sulfanyl-6-(hydroxyamino)-6-oxohexyl]amino]-2-oxoethyl]quinoline-3-carboxamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)CCCCNC(=O)CNC(=O)C1=CN=C(C=CC=C2)C2=C1 XTNMCWBPNJENRM-UHFFFAOYSA-N 0.000 claims description 2
- GNLAXPXCSPDWJP-UHFFFAOYSA-N n-[5-(4-but-2-ynoxyphenyl)sulfanyl-6-(hydroxyamino)-6-oxohexyl]-9h-xanthene-9-carboxamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)CCCCNC(=O)C1C2=CC=CC=C2OC2=CC=CC=C21 GNLAXPXCSPDWJP-UHFFFAOYSA-N 0.000 claims description 2
- HYLFDNGCOWLWAO-UHFFFAOYSA-N n-[5-(4-but-2-ynoxyphenyl)sulfinyl-6-(hydroxyamino)-6-oxohexyl]-2-(2-phenylethyl)benzamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)C(C(=O)NO)CCCCNC(=O)C1=CC=CC=C1CCC1=CC=CC=C1 HYLFDNGCOWLWAO-UHFFFAOYSA-N 0.000 claims description 2
- NBGMZPWUYKTAGS-UHFFFAOYSA-N n-[5-(4-but-2-ynoxyphenyl)sulfinyl-6-(hydroxyamino)-6-oxohexyl]quinoline-2-carboxamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)C(C(=O)NO)CCCCNC(=O)C1=CC=C(C=CC=C2)C2=N1 NBGMZPWUYKTAGS-UHFFFAOYSA-N 0.000 claims description 2
- JVPPIWAZYSSJLY-UHFFFAOYSA-N n-[5-(4-but-2-ynoxyphenyl)sulfinyl-6-(hydroxyamino)-6-oxohexyl]quinoline-3-carboxamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)C(C(=O)NO)CCCCNC(=O)C1=CN=C(C=CC=C2)C2=C1 JVPPIWAZYSSJLY-UHFFFAOYSA-N 0.000 claims description 2
- DUQFVZHDMNEFGH-UHFFFAOYSA-N n-[5-(4-but-2-ynoxyphenyl)sulfonyl-6-(hydroxyamino)-6-oxohexyl]-9h-xanthene-9-carboxamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)(=O)C(C(=O)NO)CCCCNC(=O)C1C2=CC=CC=C2OC2=CC=CC=C21 DUQFVZHDMNEFGH-UHFFFAOYSA-N 0.000 claims description 2
- XNBYYLBNAHOLJF-UHFFFAOYSA-N n-[5-(4-but-2-ynoxyphenyl)sulfonyl-6-(hydroxyamino)-6-oxohexyl]quinoline-2-carboxamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)(=O)C(C(=O)NO)CCCCNC(=O)C1=CC=C(C=CC=C2)C2=N1 XNBYYLBNAHOLJF-UHFFFAOYSA-N 0.000 claims description 2
- 229940080818 propionamide Drugs 0.000 claims description 2
- LOAUVZALPPNFOQ-UHFFFAOYSA-N quinaldic acid Chemical compound C1=CC=CC2=NC(C(=O)O)=CC=C21 LOAUVZALPPNFOQ-UHFFFAOYSA-N 0.000 claims description 2
- DJXNJVFEFSWHLY-UHFFFAOYSA-N quinoline-3-carboxylic acid Chemical compound C1=CC=CC2=CC(C(=O)O)=CN=C21 DJXNJVFEFSWHLY-UHFFFAOYSA-N 0.000 claims description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 23
- 150000002431 hydrogen Chemical class 0.000 claims 12
- 239000000203 mixture Substances 0.000 claims 9
- 238000000034 method Methods 0.000 claims 8
- 229960001171 acetohydroxamic acid Drugs 0.000 claims 7
- 239000000126 substance Substances 0.000 claims 6
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 6
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 5
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 3
- 206010007559 Cardiac failure congestive Diseases 0.000 claims 2
- 206010019280 Heart failures Diseases 0.000 claims 2
- 241000124008 Mammalia Species 0.000 claims 2
- 206010037660 Pyrexia Diseases 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
- 231100000915 pathological change Toxicity 0.000 claims 2
- 230000036285 pathological change Effects 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- XQTMJWDDXQDAKO-QYWNIODHSA-N (2r)-2-(4-but-2-ynoxyphenyl)sulfinyl-n-hydroxy-2-(4-thiophen-2-ylphenyl)acetamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)[C@@H](C(=O)NO)C1=CC=C(C=2SC=CC=2)C=C1 XQTMJWDDXQDAKO-QYWNIODHSA-N 0.000 claims 1
- LMLJZJGMFKPKNY-BPNWFJGMSA-N (2r)-2-(4-but-2-ynoxyphenyl)sulfinyl-n-hydroxy-2-phenylacetamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)[C@@H](C(=O)NO)C1=CC=CC=C1 LMLJZJGMFKPKNY-BPNWFJGMSA-N 0.000 claims 1
- YYOVZJXOBZVIQK-CKAQCJTGSA-N (2r)-2-(4-but-2-ynoxyphenyl)sulfinyl-n-hydroxy-3-methylbutanamide Chemical compound CC#CCOC1=CC=C(S(=O)[C@H](C(C)C)C(=O)NO)C=C1 YYOVZJXOBZVIQK-CKAQCJTGSA-N 0.000 claims 1
- ILAOVOOZLVGAJF-UHFFFAOYSA-N 1-methylpyrrole-2-carboxylic acid Chemical compound CN1C=CC=C1C(O)=O ILAOVOOZLVGAJF-UHFFFAOYSA-N 0.000 claims 1
- CWGOBWMKFRWKPM-UHFFFAOYSA-N 2-(1-benzoylpiperidin-4-yl)-2-(4-but-2-ynoxyphenyl)sulfonyl-n-hydroxyacetamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)(=O)C(C(=O)NO)C1CCN(C(=O)C=2C=CC=CC=2)CC1 CWGOBWMKFRWKPM-UHFFFAOYSA-N 0.000 claims 1
- YIFLAUJBDUSBJQ-UHFFFAOYSA-N 2-(3-bromophenyl)-2-(4-but-2-ynoxyphenyl)sulfonyl-n-hydroxyacetamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)(=O)C(C(=O)NO)C1=CC=CC(Br)=C1 YIFLAUJBDUSBJQ-UHFFFAOYSA-N 0.000 claims 1
- YUZYHGVJRYGNGS-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-2-(4-chlorophenyl)-n-hydroxyacetamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)C1=CC=C(Cl)C=C1 YUZYHGVJRYGNGS-UHFFFAOYSA-N 0.000 claims 1
- ILUVAAMGYFXXGD-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-2-cyclohexyl-n-hydroxyacetamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)C1CCCCC1 ILUVAAMGYFXXGD-UHFFFAOYSA-N 0.000 claims 1
- QPFIRNJZWOAQOU-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-6-[[2-(1,3-dioxoisoindol-2-yl)acetyl]amino]-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)CCCCNC(=O)CN1C(=O)C2=CC=CC=C2C1=O QPFIRNJZWOAQOU-UHFFFAOYSA-N 0.000 claims 1
- PGKIWJNJWVVWHM-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-6-[[2-[[2-(1,3-dioxoisoindol-2-yl)acetyl]amino]acetyl]amino]-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)CCCCNC(=O)CNC(=O)CN1C(=O)C2=CC=CC=C2C1=O PGKIWJNJWVVWHM-UHFFFAOYSA-N 0.000 claims 1
- ALADMWIXYJPORU-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-6-[[2-[[2-(3,4-dichlorophenyl)acetyl]amino]acetyl]amino]-n-hydroxyhexanamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)CCCCNC(=O)CNC(=O)CC1=CC=C(Cl)C(Cl)=C1 ALADMWIXYJPORU-UHFFFAOYSA-N 0.000 claims 1
- RGROQXWBAZRUAV-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-N-hydroxyacetamide Chemical compound CC#CCOC1=CC=C(C=C1)SCC(=O)NO RGROQXWBAZRUAV-UHFFFAOYSA-N 0.000 claims 1
- VEMPUXZNKSUVFD-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-n-hydroxy-2-(4-methoxyphenyl)acetamide Chemical compound C1=CC(OC)=CC=C1C(C(=O)NO)SC1=CC=C(OCC#CC)C=C1 VEMPUXZNKSUVFD-UHFFFAOYSA-N 0.000 claims 1
- QURIEHRBDDARFL-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-n-hydroxy-2-naphthalen-2-ylacetamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)C1=CC=C(C=CC=C2)C2=C1 QURIEHRBDDARFL-UHFFFAOYSA-N 0.000 claims 1
- CDIBBFPULKXHGN-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-n-hydroxy-2-phenylacetamide Chemical compound C1=CC(OCC#CC)=CC=C1SC(C(=O)NO)C1=CC=CC=C1 CDIBBFPULKXHGN-UHFFFAOYSA-N 0.000 claims 1
- JUKIJVGLFPZICB-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfanyl-n-hydroxy-3-methylbutanamide Chemical compound CC#CCOC1=CC=C(SC(C(C)C)C(=O)NO)C=C1 JUKIJVGLFPZICB-UHFFFAOYSA-N 0.000 claims 1
- LMVMXGLSCFFZIQ-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfinyl-2-(4-chlorophenyl)-n-hydroxyacetamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)C(C(=O)NO)C1=CC=C(Cl)C=C1 LMVMXGLSCFFZIQ-UHFFFAOYSA-N 0.000 claims 1
- YUUBFIMJZZUFNO-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfinyl-2-(4-fluorophenyl)-n-hydroxyacetamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)C(C(=O)NO)C1=CC=C(F)C=C1 YUUBFIMJZZUFNO-UHFFFAOYSA-N 0.000 claims 1
- YAOLTEPPKVIFGN-UHFFFAOYSA-N 2-(4-but-2-ynoxyphenyl)sulfinyl-2-cyclohexyl-n-hydroxyacetamide Chemical compound C1=CC(OCC#CC)=CC=C1S(=O)C(C(=O)NO)C1CCCCC1 YAOLTEPPKVIFGN-UHFFFAOYSA-N 0.000 claims 1
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
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- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/60—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
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- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/34—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/56—Amides
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- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
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- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
- C07D217/06—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with the ring nitrogen atom acylated by carboxylic or carbonic acids, or with sulfur or nitrogen analogues thereof, e.g. carbamates
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- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
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- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/04—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
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- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/78—Ring systems having three or more relevant rings
- C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
- C07D311/82—Xanthenes
- C07D311/84—Xanthenes with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 9
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- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/54—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D333/60—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C07D335/00—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom
- C07D335/04—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
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- Chemical & Material Sciences (AREA)
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- Pyrane Compounds (AREA)
- Pyrrole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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Applications Claiming Priority (1)
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US23908899A | 1999-01-27 | 1999-01-27 |
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ZA200105066A ZA200105066B (en) | 1999-01-27 | 2001-06-20 | Alkynyl containing hydroxamic acid compounds as TACE inhibitors. |
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EP (1) | EP1147080B1 (ru) |
JP (1) | JP2002535384A (ru) |
KR (1) | KR20010101689A (ru) |
CN (1) | CN1183107C (ru) |
AR (1) | AR035311A1 (ru) |
AT (1) | ATE271541T1 (ru) |
AU (1) | AU767754B2 (ru) |
BR (1) | BR0007783A (ru) |
CA (1) | CA2356346A1 (ru) |
CZ (1) | CZ20012707A3 (ru) |
DE (1) | DE60012303T2 (ru) |
DK (1) | DK1147080T3 (ru) |
EA (1) | EA004883B1 (ru) |
ES (1) | ES2225104T3 (ru) |
HK (1) | HK1037611A1 (ru) |
HU (1) | HUP0200213A3 (ru) |
IL (1) | IL144348A0 (ru) |
NO (1) | NO20013677L (ru) |
NZ (1) | NZ512446A (ru) |
PL (1) | PL349042A1 (ru) |
PT (1) | PT1147080E (ru) |
WO (1) | WO2000044713A1 (ru) |
ZA (1) | ZA200105066B (ru) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
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GB9918684D0 (en) | 1999-08-09 | 1999-10-13 | Novartis Ag | Organic compounds |
DE10015533A1 (de) * | 1999-11-30 | 2001-06-28 | Rohmax Additives Gmbh | Blockcopolymere sowie Verfahren zur Hestellung und Verwendung |
DK1335898T3 (da) * | 2000-09-29 | 2006-04-03 | Topotarget Uk Ltd | Carbaminsyreforbindelser omfattende en amidbinding som HDAC-inhibitorer |
GB0103303D0 (en) | 2001-02-09 | 2001-03-28 | Novartis Ag | Organic compounds |
WO2003022801A1 (fr) * | 2001-09-07 | 2003-03-20 | Kaken Pharmaceutical Co., Ltd. | Derives d'acide hydroxamique inverse |
JP2003081838A (ja) * | 2001-09-11 | 2003-03-19 | Rohto Pharmaceut Co Ltd | グルコサミン製剤 |
US7199155B2 (en) | 2002-12-23 | 2007-04-03 | Wyeth Holdings Corporation | Acetylenic aryl sulfonate hydroxamic acid TACE and matrix metalloproteinase inhibitors |
KR101312993B1 (ko) * | 2006-10-28 | 2013-11-25 | 엔비보 파마슈티칼즈, 인코퍼레이티드 | 히스톤 데아세틸라아제의 억제제 |
ES2428326T3 (es) * | 2007-10-04 | 2013-11-07 | Merck Sharp & Dohme Corp. | Derivados de aril sulfona sustituida como bloqueadores de canales de calcio |
GB201008047D0 (en) * | 2010-05-14 | 2010-06-30 | Ge Healthcare Ltd | Method of synthesis |
WO2012036257A1 (ja) * | 2010-09-17 | 2012-03-22 | 国立大学法人東京大学 | 血小板の機能を維持するための組成物 |
CR20160472A (es) | 2014-04-11 | 2017-03-10 | Viiv Healthcare Uk (No 4) Ltd | Triterpenoides con actividad inhibidora de la maduración del vih |
US10724025B2 (en) * | 2016-05-05 | 2020-07-28 | Codexis, Inc. | Penicillin-G acylases |
US20210393632A1 (en) | 2018-10-04 | 2021-12-23 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Egfr inhibitors for treating keratodermas |
Family Cites Families (2)
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WO1998016514A1 (en) * | 1996-10-16 | 1998-04-23 | American Cyanamid Company | Ortho-sulfonamido bicyclic heteroaryl hydroxamic acids as matrix metalloproteinase and tace inhibitors |
DE69823019T2 (de) * | 1997-02-27 | 2005-03-31 | Wyeth Holdings Corp. | N-hydroxy-2-(alkyl, aryl oder heteroaryl sulfanyl, sulfinyl oder sulfonyl)-3-substituierte alkyl-, aryl- oder heteroarylamide als matrixmetalloproteinaseinhibitoren |
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2000
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2001
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HK1037611A1 (en) | 2002-02-15 |
PL349042A1 (en) | 2002-07-01 |
EP1147080A1 (en) | 2001-10-24 |
NZ512446A (en) | 2004-02-27 |
CA2356346A1 (en) | 2000-08-03 |
NO20013677L (no) | 2001-09-20 |
HUP0200213A2 (en) | 2002-06-29 |
KR20010101689A (ko) | 2001-11-14 |
EA200100807A1 (ru) | 2002-08-29 |
CN1337945A (zh) | 2002-02-27 |
CZ20012707A3 (cs) | 2002-05-15 |
DK1147080T3 (da) | 2004-09-27 |
ATE271541T1 (de) | 2004-08-15 |
AR035311A1 (es) | 2004-05-12 |
BR0007783A (pt) | 2002-02-05 |
JP2002535384A (ja) | 2002-10-22 |
NO20013677D0 (no) | 2001-07-26 |
DE60012303D1 (de) | 2004-08-26 |
AU3351500A (en) | 2000-08-18 |
ES2225104T3 (es) | 2005-03-16 |
EA004883B1 (ru) | 2004-08-26 |
IL144348A0 (en) | 2002-05-23 |
HUP0200213A3 (en) | 2005-04-28 |
DE60012303T2 (de) | 2005-07-28 |
EP1147080B1 (en) | 2004-07-21 |
WO2000044713A1 (en) | 2000-08-03 |
CN1183107C (zh) | 2005-01-05 |
PT1147080E (pt) | 2004-11-30 |
AU767754B2 (en) | 2003-11-20 |
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