CA2366800A1 - Derives de l'acide carboxylique qui inhibent la liaison d'integrines a leurs recepteurs - Google Patents
Derives de l'acide carboxylique qui inhibent la liaison d'integrines a leurs recepteurs Download PDFInfo
- Publication number
- CA2366800A1 CA2366800A1 CA 2366800 CA2366800A CA2366800A1 CA 2366800 A1 CA2366800 A1 CA 2366800A1 CA 2366800 CA2366800 CA 2366800 CA 2366800 A CA2366800 A CA 2366800A CA 2366800 A1 CA2366800 A1 CA 2366800A1
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- CA
- Canada
- Prior art keywords
- amino
- alkyl
- dihydro
- carbonyl
- oxo
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 102000006495 integrins Human genes 0.000 title claims abstract 3
- 108010044426 integrins Proteins 0.000 title claims abstract 3
- 102000005962 receptors Human genes 0.000 title abstract 2
- 108020003175 receptors Proteins 0.000 title abstract 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 31
- 238000000034 method Methods 0.000 claims abstract 2
- -1 aliphatic acyl Chemical group 0.000 claims 126
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 89
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 39
- 125000003118 aryl group Chemical group 0.000 claims 39
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 36
- 125000000217 alkyl group Chemical group 0.000 claims 35
- 125000003710 aryl alkyl group Chemical group 0.000 claims 27
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 27
- 229910052739 hydrogen Inorganic materials 0.000 claims 26
- 239000001257 hydrogen Substances 0.000 claims 26
- 125000000623 heterocyclic group Chemical group 0.000 claims 24
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 24
- 125000002877 alkyl aryl group Chemical group 0.000 claims 23
- 125000000753 cycloalkyl group Chemical group 0.000 claims 22
- 125000001188 haloalkyl group Chemical group 0.000 claims 22
- 125000003342 alkenyl group Chemical group 0.000 claims 21
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 21
- 125000000304 alkynyl group Chemical group 0.000 claims 21
- 125000005160 aryl oxy alkyl group Chemical group 0.000 claims 21
- 150000005347 biaryls Chemical group 0.000 claims 21
- 150000003857 carboxamides Chemical class 0.000 claims 21
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 21
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 21
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 21
- MBVFRSJFKMJRHA-UHFFFAOYSA-N 4-fluoro-1-benzofuran-7-carbaldehyde Chemical compound FC1=CC=C(C=O)C2=C1C=CO2 MBVFRSJFKMJRHA-UHFFFAOYSA-N 0.000 claims 20
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 20
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims 20
- 125000006319 alkynyl amino group Chemical group 0.000 claims 20
- 125000003435 aroyl group Chemical group 0.000 claims 20
- 125000001769 aryl amino group Chemical group 0.000 claims 20
- 125000004104 aryloxy group Chemical group 0.000 claims 20
- 125000004986 diarylamino group Chemical group 0.000 claims 20
- 125000005000 thioaryl group Chemical group 0.000 claims 20
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 16
- 229910018828 PO3H2 Inorganic materials 0.000 claims 15
- 125000003545 alkoxy group Chemical group 0.000 claims 14
- 229910052736 halogen Inorganic materials 0.000 claims 14
- 150000002367 halogens Chemical class 0.000 claims 14
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims 14
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 14
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 13
- 125000006323 alkenyl amino group Chemical group 0.000 claims 13
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 13
- 125000003282 alkyl amino group Chemical group 0.000 claims 13
- 229910052799 carbon Inorganic materials 0.000 claims 13
- 125000005309 thioalkoxy group Chemical group 0.000 claims 13
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 12
- 150000002431 hydrogen Chemical class 0.000 claims 12
- 229910052760 oxygen Inorganic materials 0.000 claims 12
- 150000003839 salts Chemical class 0.000 claims 11
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims 9
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 9
- 235000019260 propionic acid Nutrition 0.000 claims 9
- 125000006575 electron-withdrawing group Chemical group 0.000 claims 8
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 7
- YKOWBJJOJNGCAD-SHYZEUOFSA-N [(2r,3s,5r)-3-hydroxy-5-[4-(hydroxyamino)-2-oxopyrimidin-1-yl]oxolan-2-yl]methyl dihydrogen phosphate Chemical compound O=C1N=C(NO)C=CN1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)C1 YKOWBJJOJNGCAD-SHYZEUOFSA-N 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- 229910052717 sulfur Inorganic materials 0.000 claims 7
- 150000001408 amides Chemical class 0.000 claims 6
- 150000007854 aminals Chemical class 0.000 claims 6
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 6
- 150000004657 carbamic acid derivatives Chemical class 0.000 claims 6
- 150000002148 esters Chemical class 0.000 claims 6
- 230000003287 optical effect Effects 0.000 claims 6
- 229940002612 prodrug Drugs 0.000 claims 6
- 239000000651 prodrug Substances 0.000 claims 6
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 claims 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 241000124008 Mammalia Species 0.000 claims 2
- YJBZUNGDVIZBHK-FQEVSTJZSA-N (3s)-3-(1,3-benzodioxol-5-yl)-3-[(1-benzyl-2-oxo-4-propylpyridin-3-yl)carbamoylamino]propanoic acid Chemical compound O=C1C(NC(=O)N[C@@H](CC(O)=O)C=2C=C3OCOC3=CC=2)=C(CCC)C=CN1CC1=CC=CC=C1 YJBZUNGDVIZBHK-FQEVSTJZSA-N 0.000 claims 1
- NPLRMHVUHIXNOI-SFHVURJKSA-N (3s)-3-(1,3-benzodioxol-5-yl)-3-[[2-oxo-1-[[4-(trifluoromethyl)phenyl]methyl]pyridin-3-yl]carbamoylamino]propanoic acid Chemical compound N([C@@H](CC(=O)O)C=1C=C2OCOC2=CC=1)C(=O)NC(C1=O)=CC=CN1CC1=CC=C(C(F)(F)F)C=C1 NPLRMHVUHIXNOI-SFHVURJKSA-N 0.000 claims 1
- VJBPWWKJTWLJRH-NRFANRHFSA-N (3s)-3-(3-butoxyphenyl)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]propanoic acid Chemical compound CCCCOC1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=CC=2O)=O)=C1 VJBPWWKJTWLJRH-NRFANRHFSA-N 0.000 claims 1
- ZRKLOPALDUJTRE-SANMLTNESA-N (3s)-3-[(1-benzyl-6-methyl-2-oxo-4-phenylmethoxypyridin-3-yl)carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C(N(CC=1C=CC=CC=1)C(C)=C1)=O)=C1OCC1=CC=CC=C1 ZRKLOPALDUJTRE-SANMLTNESA-N 0.000 claims 1
- RUEWEKYBQZCWRD-FQEVSTJZSA-N (3s)-3-[[1-[(2,4-dichlorophenyl)methyl]-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=CC=CN1CC1=CC=C(Cl)C=C1Cl RUEWEKYBQZCWRD-FQEVSTJZSA-N 0.000 claims 1
- QQWKDWJISNTBNF-FQEVSTJZSA-N (3s)-3-[[1-[(2-bromophenyl)methyl]-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=CC=CN1CC1=CC=CC=C1Br QQWKDWJISNTBNF-FQEVSTJZSA-N 0.000 claims 1
- HRQHUYXBRUCBES-FQEVSTJZSA-N (3s)-3-[[1-[(2-bromophenyl)methyl]-4-methyl-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(C)C=CN1CC1=CC=CC=C1Br HRQHUYXBRUCBES-FQEVSTJZSA-N 0.000 claims 1
- MKIYRELWYFXDNI-IBGZPJMESA-N (3s)-3-[[1-[(2-chloro-5-methylsulfonylphenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=CC(S(C)(=O)=O)=CC=C1Cl MKIYRELWYFXDNI-IBGZPJMESA-N 0.000 claims 1
- LRVLEACHUMEARV-IBGZPJMESA-N (3s)-3-[[1-[(2-chloro-6-cyanophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=C(Cl)C=CC=C1C#N LRVLEACHUMEARV-IBGZPJMESA-N 0.000 claims 1
- SZTLQNNZZKOUFZ-DEOSSOPVSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-(3,5-diethoxyphenyl)propanoic acid Chemical compound CCOC1=CC(OCC)=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3Cl)OCC)C=3CCCC=3C=2O)=O)=C1 SZTLQNNZZKOUFZ-DEOSSOPVSA-N 0.000 claims 1
- VVPRFVSNKFXSAA-QHCPKHFHSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-(3-propoxyphenyl)propanoic acid Chemical compound CCCOC1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3Cl)OCC)C=3CCCC=3C=2O)=O)=C1 VVPRFVSNKFXSAA-QHCPKHFHSA-N 0.000 claims 1
- KKUFMTRHHSKNSC-DEOSSOPVSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-[3-(cyclopropylmethoxy)phenyl]propanoic acid Chemical compound CCOC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)N[C@@H](CC(O)=O)C=2C=C(OCC3CC3)C=CC=2)=C(O)C2=C1CCC2 KKUFMTRHHSKNSC-DEOSSOPVSA-N 0.000 claims 1
- BCAIQXAJAJOICN-FQEVSTJZSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-phenylpropanoic acid Chemical compound CCOC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)N[C@@H](CC(O)=O)C=2C=CC=CC=2)=C(O)C2=C1CCC2 BCAIQXAJAJOICN-FQEVSTJZSA-N 0.000 claims 1
- CXCIRZSCPRQHIY-FQEVSTJZSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3-ethoxyphenyl)propanoic acid Chemical compound CCOC1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3Cl)OCC)C=CC=2O)=O)=C1 CXCIRZSCPRQHIY-FQEVSTJZSA-N 0.000 claims 1
- HWIOCUIUIQNYHM-NRFANRHFSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3-propan-2-yloxyphenyl)propanoic acid Chemical compound CCOC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)N[C@@H](CC(O)=O)C=2C=C(OC(C)C)C=CC=2)=C(O)C=C1 HWIOCUIUIQNYHM-NRFANRHFSA-N 0.000 claims 1
- PYNIBSQZENUKGC-QHCPKHFHSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-5,6-dimethyl-2-oxopyridin-3-yl]carbamoylamino]-3-(3-propan-2-yloxyphenyl)propanoic acid Chemical compound CCOC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)N[C@@H](CC(O)=O)C=2C=C(OC(C)C)C=CC=2)=C(O)C(C)=C1C PYNIBSQZENUKGC-QHCPKHFHSA-N 0.000 claims 1
- UTEHJTXSQYHRFV-NRFANRHFSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-5-methyl-2-oxopyridin-3-yl]carbamoylamino]-3-(1-methylindol-6-yl)propanoic acid Chemical compound CCOC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)N[C@@H](CC(O)=O)C=2C=C3N(C)C=CC3=CC=2)=C(O)C(C)=C1 UTEHJTXSQYHRFV-NRFANRHFSA-N 0.000 claims 1
- YJZHCBKFNHEAOV-FQEVSTJZSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-5-methyl-2-oxopyridin-3-yl]carbamoylamino]-3-(2,3-dihydro-1-benzofuran-5-yl)propanoic acid Chemical compound CCOC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)N[C@@H](CC(O)=O)C=2C=C3CCOC3=CC=2)=C(O)C(C)=C1 YJZHCBKFNHEAOV-FQEVSTJZSA-N 0.000 claims 1
- KVAPJFYQGHCQQT-NRFANRHFSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-5-methyl-2-oxopyridin-3-yl]carbamoylamino]-3-(3-ethoxyphenyl)propanoic acid Chemical compound CCOC1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3Cl)OCC)C=C(C)C=2O)=O)=C1 KVAPJFYQGHCQQT-NRFANRHFSA-N 0.000 claims 1
- GTIAZEYFROWHCV-QFIPXVFZSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-6-methyl-2-oxopyridin-3-yl]carbamoylamino]-3-(3-propan-2-yloxyphenyl)propanoic acid Chemical compound CCOC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)N[C@@H](CC(O)=O)C=2C=C(OC(C)C)C=CC=2)=C(O)C=C1C GTIAZEYFROWHCV-QFIPXVFZSA-N 0.000 claims 1
- LMEDPEPCALCRTO-DEOSSOPVSA-N (3s)-3-[[1-[(2-chloro-6-ethoxyphenyl)methyl]-5-cyclopropyl-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3-propan-2-yloxyphenyl)propanoic acid Chemical compound CCOC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)N[C@@H](CC(O)=O)C=2C=C(OC(C)C)C=CC=2)=C(O)C(C2CC2)=C1 LMEDPEPCALCRTO-DEOSSOPVSA-N 0.000 claims 1
- WMKLRNMTKRPGEL-FQEVSTJZSA-N (3s)-3-[[1-[(2-chloro-6-fluorophenyl)methyl]-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=CC=CN1CC1=C(F)C=CC=C1Cl WMKLRNMTKRPGEL-FQEVSTJZSA-N 0.000 claims 1
- CEAOPVIFGJTFDW-SFHVURJKSA-N (3s)-3-[[1-[(2-chloro-6-fluorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=C(F)C=CC=C1Cl CEAOPVIFGJTFDW-SFHVURJKSA-N 0.000 claims 1
- XLPPWZVLRGAWAJ-FQEVSTJZSA-N (3s)-3-[[1-[(2-chloro-6-methoxyphenyl)methyl]-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound COC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)N[C@@H](CC(O)=O)C=2C=CC(C)=CC=2)=CC=C1 XLPPWZVLRGAWAJ-FQEVSTJZSA-N 0.000 claims 1
- ACJZDECYIBKQNS-IBGZPJMESA-N (3s)-3-[[1-[(2-chloro-6-methoxyphenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3,5-dimethoxyphenyl)propanoic acid Chemical compound COC1=CC(OC)=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3Cl)OC)C=CC=2O)=O)=C1 ACJZDECYIBKQNS-IBGZPJMESA-N 0.000 claims 1
- KOACDKYITDQTOG-SFHVURJKSA-N (3s)-3-[[1-[(2-chloro-6-methoxyphenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound COC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)N[C@@H](CC(O)=O)C=2C=CC(C)=CC=2)=C(O)C=C1 KOACDKYITDQTOG-SFHVURJKSA-N 0.000 claims 1
- ZMMRQNCKFDFQTL-QFIPXVFZSA-N (3s)-3-[[1-[(2-chloro-6-methylphenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-(3-ethoxyphenyl)propanoic acid Chemical compound CCOC1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3C)Cl)C=3CCCC=3C=2O)=O)=C1 ZMMRQNCKFDFQTL-QFIPXVFZSA-N 0.000 claims 1
- NLDVIGYYKODKGL-NRFANRHFSA-N (3s)-3-[[1-[(2-chloro-6-methylphenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-[3-(methanesulfonamido)phenyl]propanoic acid Chemical compound CC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)N[C@@H](CC(O)=O)C=2C=C(NS(C)(=O)=O)C=CC=2)=C(O)C2=C1CCC2 NLDVIGYYKODKGL-NRFANRHFSA-N 0.000 claims 1
- ZFKJUHAPJJWBIX-QFIPXVFZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-2-oxo-4-(propylamino)pyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound O=C1C(NC(=O)N[C@@H](CC(O)=O)C=2C=CC(C)=CC=2)=C(NCCC)C=CN1CC1=CC=CC=C1Cl ZFKJUHAPJJWBIX-QFIPXVFZSA-N 0.000 claims 1
- LLPUNNOFVNYJJQ-VWLOTQADSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-2-oxo-4-phenylpyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(C=2C=CC=CC=2)C=CN1CC1=CC=CC=C1Cl LLPUNNOFVNYJJQ-VWLOTQADSA-N 0.000 claims 1
- XJBLYQPDBGBSNJ-QFIPXVFZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-2-oxo-4-propylpyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound O=C1C(NC(=O)N[C@@H](CC(O)=O)C=2C=CC(C)=CC=2)=C(CCC)C=CN1CC1=CC=CC=C1Cl XJBLYQPDBGBSNJ-QFIPXVFZSA-N 0.000 claims 1
- GNCHCKVTNJDZDQ-QFIPXVFZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-(2,2-dimethylpropanoylamino)-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(NC(=O)C(C)(C)C)C=CN1CC1=CC=CC=C1Cl GNCHCKVTNJDZDQ-QFIPXVFZSA-N 0.000 claims 1
- KZNYVVVWALITCR-QHCPKHFHSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-(4-methylpiperazin-1-yl)-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1CN(C)CCN1C1=C(NC(=O)N[C@@H](CC(O)=O)C=2C=CC(C)=CC=2)C(=O)N(CC=2C(=CC=CC=2)Cl)C=C1 KZNYVVVWALITCR-QHCPKHFHSA-N 0.000 claims 1
- NFFRXLAVOWNYID-QHCPKHFHSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-[2-(2-methoxyethoxy)ethoxy]-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound O=C1C(NC(=O)N[C@@H](CC(O)=O)C=2C=CC(C)=CC=2)=C(OCCOCCOC)C=CN1CC1=CC=CC=C1Cl NFFRXLAVOWNYID-QHCPKHFHSA-N 0.000 claims 1
- KMNQKWXOKWWKQR-VWLOTQADSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound O=C1C(NC(=O)N[C@@H](CC(O)=O)C=2C=CC(C)=CC=2)=C(OCCOCCOCCOC)C=CN1CC1=CC=CC=C1Cl KMNQKWXOKWWKQR-VWLOTQADSA-N 0.000 claims 1
- BNRMVPBVZOZNMK-QFIPXVFZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-(1-ethylindol-5-yl)propanoic acid Chemical compound N([C@@H](CC(O)=O)C=1C=C2C=CN(C2=CC=1)CC)C(=O)NC(C1=O)=C(O)C=2CCCC=2N1CC1=CC=CC=C1Cl BNRMVPBVZOZNMK-QFIPXVFZSA-N 0.000 claims 1
- MGQINSKBDBVSJS-NRFANRHFSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-(1-methylindol-5-yl)propanoic acid Chemical compound N([C@@H](CC(O)=O)C=1C=C2C=CN(C2=CC=1)C)C(=O)NC(C1=O)=C(O)C=2CCCC=2N1CC1=CC=CC=C1Cl MGQINSKBDBVSJS-NRFANRHFSA-N 0.000 claims 1
- DHHNPZIXYMWDPH-NRFANRHFSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-(3,5-dimethylphenyl)propanoic acid Chemical compound CC1=CC(C)=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=3CCCC=3C=2O)=O)=C1 DHHNPZIXYMWDPH-NRFANRHFSA-N 0.000 claims 1
- LUUUHVOTVYSQFF-FQEVSTJZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-(3-methylphenyl)propanoic acid Chemical compound CC1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=3CCCC=3C=2O)=O)=C1 LUUUHVOTVYSQFF-FQEVSTJZSA-N 0.000 claims 1
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- YGYUTUJPVHUXJW-FQEVSTJZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C(N1CC=2C(=CC=CC=2)Cl)=O)=C(O)C2=C1CCC2 YGYUTUJPVHUXJW-FQEVSTJZSA-N 0.000 claims 1
- OERFSFLUEDUFJD-IBGZPJMESA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]propanoic acid Chemical compound N([C@@H](CC(=O)O)C=1C=C(OC(F)(F)C(F)F)C=CC=1)C(=O)NC(C1=O)=C(O)C=2CCCC=2N1CC1=CC=CC=C1Cl OERFSFLUEDUFJD-IBGZPJMESA-N 0.000 claims 1
- HADSFMDFAUFDGC-QHCPKHFHSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-[3-(diethylamino)phenyl]propanoic acid Chemical compound CCN(CC)C1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=3CCCC=3C=2O)=O)=C1 HADSFMDFAUFDGC-QHCPKHFHSA-N 0.000 claims 1
- BDLHJEJKWOYMAT-IBGZPJMESA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxo-6,7-dihydro-5h-cyclopenta[b]pyridin-3-yl]carbamoylamino]-3-[3-(difluoromethoxy)phenyl]propanoic acid Chemical compound N([C@@H](CC(=O)O)C=1C=C(OC(F)F)C=CC=1)C(=O)NC(C1=O)=C(O)C=2CCCC=2N1CC1=CC=CC=C1Cl BDLHJEJKWOYMAT-IBGZPJMESA-N 0.000 claims 1
- IMNHTTFOXQVWMA-IBGZPJMESA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3,4-diethoxyphenyl)propanoic acid Chemical compound C1=C(OCC)C(OCC)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1Cl IMNHTTFOXQVWMA-IBGZPJMESA-N 0.000 claims 1
- WZWLVJNBDJRATC-KRWDZBQOSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3,4-dimethoxyphenyl)propanoic acid Chemical compound C1=C(OC)C(OC)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1Cl WZWLVJNBDJRATC-KRWDZBQOSA-N 0.000 claims 1
- WXJXZGFTBHUTRC-NRFANRHFSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3,4-dipropoxyphenyl)propanoic acid Chemical compound C1=C(OCCC)C(OCCC)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1Cl WXJXZGFTBHUTRC-NRFANRHFSA-N 0.000 claims 1
- NOJGFYRCCNSGFU-SFHVURJKSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3,5-dimethoxy-4-methylphenyl)propanoic acid Chemical compound COC1=C(C)C(OC)=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=CC=2O)=O)=C1 NOJGFYRCCNSGFU-SFHVURJKSA-N 0.000 claims 1
- WGCGJUIUYDXFGN-IBGZPJMESA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3,5-dimethoxyphenyl)propanoic acid Chemical compound COC1=CC(OC)=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=CC=2O)=O)=C1 WGCGJUIUYDXFGN-IBGZPJMESA-N 0.000 claims 1
- JPEASVDUPDPZHB-IBGZPJMESA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3,5-dimethylphenyl)propanoic acid Chemical compound CC1=CC(C)=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=CC=2O)=O)=C1 JPEASVDUPDPZHB-IBGZPJMESA-N 0.000 claims 1
- JEIDCRKRGJNGEE-SFHVURJKSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3-ethoxy-4-methoxyphenyl)propanoic acid Chemical compound C1=C(OC)C(OCC)=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=CC=2O)=O)=C1 JEIDCRKRGJNGEE-SFHVURJKSA-N 0.000 claims 1
- NFUAGYQZSQRSIE-SFHVURJKSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3-methoxy-4-methylphenyl)propanoic acid Chemical compound C1=C(C)C(OC)=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=CC=2O)=O)=C1 NFUAGYQZSQRSIE-SFHVURJKSA-N 0.000 claims 1
- NWPNNXYHAUHECQ-SFHVURJKSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3-methylphenyl)propanoic acid Chemical compound CC1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=CC=2O)=O)=C1 NWPNNXYHAUHECQ-SFHVURJKSA-N 0.000 claims 1
- HYYLDLOGMRYXKL-FQEVSTJZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3-propan-2-yloxyphenyl)propanoic acid Chemical compound CC(C)OC1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=CC=2O)=O)=C1 HYYLDLOGMRYXKL-FQEVSTJZSA-N 0.000 claims 1
- JNBGWQREIHPHSK-SFHVURJKSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methoxy-3-methylphenyl)propanoic acid Chemical compound C1=C(C)C(OC)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1Cl JNBGWQREIHPHSK-SFHVURJKSA-N 0.000 claims 1
- ICYAAIQHXXAWGE-SFHVURJKSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methoxyphenyl)propanoic acid Chemical compound C1=CC(OC)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1Cl ICYAAIQHXXAWGE-SFHVURJKSA-N 0.000 claims 1
- LPMXAWSSWLCPMJ-SFHVURJKSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1Cl LPMXAWSSWLCPMJ-SFHVURJKSA-N 0.000 claims 1
- KAFPTYJJRUUWDY-INIZCTEOSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(7-methoxy-1,3-benzodioxol-5-yl)propanoic acid Chemical compound N([C@@H](CC(O)=O)C=1C=C(C=2OCOC=2C=1)OC)C(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1Cl KAFPTYJJRUUWDY-INIZCTEOSA-N 0.000 claims 1
- STILENFGKGREPY-KRWDZBQOSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-[3-(difluoromethoxy)phenyl]propanoic acid Chemical compound N([C@@H](CC(=O)O)C=1C=C(OC(F)F)C=CC=1)C(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1Cl STILENFGKGREPY-KRWDZBQOSA-N 0.000 claims 1
- PAMQUYCMYTUMJW-KRWDZBQOSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-[3-(trifluoromethyl)phenyl]propanoic acid Chemical compound N([C@@H](CC(=O)O)C=1C=C(C=CC=1)C(F)(F)F)C(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1Cl PAMQUYCMYTUMJW-KRWDZBQOSA-N 0.000 claims 1
- SVJORHDCZSSIIV-KRWDZBQOSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-phenylpropanoic acid Chemical compound N([C@@H](CC(=O)O)C=1C=CC=CC=1)C(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1Cl SVJORHDCZSSIIV-KRWDZBQOSA-N 0.000 claims 1
- VPUXZZJIKIIVKJ-NRFANRHFSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxoquinolin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C2=CC=CC=C2N1CC1=CC=CC=C1Cl VPUXZZJIKIIVKJ-NRFANRHFSA-N 0.000 claims 1
- AJZJNWQCAWBSAM-FQEVSTJZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-5-methyl-2-oxopyridin-3-yl]carbamoylamino]-3-(3-ethoxyphenyl)propanoic acid Chemical compound CCOC1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=C(C)C=2O)=O)=C1 AJZJNWQCAWBSAM-FQEVSTJZSA-N 0.000 claims 1
- JRGSXHUFFDTFCN-IBGZPJMESA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-5-methyl-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C(C)=CN1CC1=CC=CC=C1Cl JRGSXHUFFDTFCN-IBGZPJMESA-N 0.000 claims 1
- WGJZFXOBILLYRU-QFIPXVFZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-5-methyl-2-oxopyridin-3-yl]carbamoylamino]-3-[3-(diethylamino)phenyl]propanoic acid Chemical compound CCN(CC)C1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3)Cl)C=C(C)C=2O)=O)=C1 WGJZFXOBILLYRU-QFIPXVFZSA-N 0.000 claims 1
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- JFXXBRDNTIWECS-NRFANRHFSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-methyl-2-oxopyridin-3-yl]carbamoylamino]-3-(3,4-dimethylphenyl)propanoic acid Chemical compound C1=C(C)C(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(C)C=CN1CC1=CC=CC=C1Cl JFXXBRDNTIWECS-NRFANRHFSA-N 0.000 claims 1
- DTSFNLOQTZNOMO-FQEVSTJZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-methyl-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methoxyphenyl)propanoic acid Chemical compound C1=CC(OC)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(C)C=CN1CC1=CC=CC=C1Cl DTSFNLOQTZNOMO-FQEVSTJZSA-N 0.000 claims 1
- FEUBKIVRGLIYSQ-QFIPXVFZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-4-morpholin-4-yl-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(N2CCOCC2)C=CN1CC1=CC=CC=C1Cl FEUBKIVRGLIYSQ-QFIPXVFZSA-N 0.000 claims 1
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- XEHDSQSMOHDBQB-FQEVSTJZSA-N (3s)-3-[[1-[(2-chlorophenyl)methyl]-5-methyl-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=CC(C)=CN1CC1=CC=CC=C1Cl XEHDSQSMOHDBQB-FQEVSTJZSA-N 0.000 claims 1
- IKFWKNWZMBVMRO-FQEVSTJZSA-N (3s)-3-[[1-[(2-fluorophenyl)methyl]-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=CC=CN1CC1=CC=CC=C1F IKFWKNWZMBVMRO-FQEVSTJZSA-N 0.000 claims 1
- YYPZHWRKAVHZNN-SFHVURJKSA-N (3s)-3-[[1-[(2-fluorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1F YYPZHWRKAVHZNN-SFHVURJKSA-N 0.000 claims 1
- IUXRXXOVPXHPAB-SFHVURJKSA-N (3s)-3-[[1-[(4-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=CC=C(Cl)C=C1 IUXRXXOVPXHPAB-SFHVURJKSA-N 0.000 claims 1
- JIYRLYKPKAOWDE-QFIPXVFZSA-N (3s)-3-[[1-benzyl-2-methyl-4-(2-methylpropyl)-6-oxopyrimidin-5-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound O=C1C(NC(=O)N[C@@H](CC(O)=O)C=2C=CC(C)=CC=2)=C(CC(C)C)N=C(C)N1CC1=CC=CC=C1 JIYRLYKPKAOWDE-QFIPXVFZSA-N 0.000 claims 1
- MGZUXMWNUQSKLO-NRFANRHFSA-N (3s)-3-[[4-(azetidin-1-yl)-1-[(2-chlorophenyl)methyl]-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(N2CCC2)C=CN1CC1=CC=CC=C1Cl MGZUXMWNUQSKLO-NRFANRHFSA-N 0.000 claims 1
- PLYPHUVVZDVHLW-QFIPXVFZSA-N (3s)-3-[[4-(tert-butylcarbamoylamino)-1-[(2-chlorophenyl)methyl]-2-oxopyridin-3-yl]carbamoylamino]-3-(4-methylphenyl)propanoic acid Chemical compound C1=CC(C)=CC=C1[C@H](CC(O)=O)NC(=O)NC(C1=O)=C(NC(=O)NC(C)(C)C)C=CN1CC1=CC=CC=C1Cl PLYPHUVVZDVHLW-QFIPXVFZSA-N 0.000 claims 1
- IRHRRVMOJWKLGL-FQEVSTJZSA-N (3s)-3-[[5-chloro-1-[(2-chloro-6-ethoxyphenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-(3-ethoxyphenyl)propanoic acid Chemical compound CCOC1=CC=CC([C@H](CC(O)=O)NC(=O)NC=2C(N(CC=3C(=CC=CC=3Cl)OCC)C=C(Cl)C=2O)=O)=C1 IRHRRVMOJWKLGL-FQEVSTJZSA-N 0.000 claims 1
- UUDALWDRIFYZPM-UHFFFAOYSA-N 1h-pyridine-2,4-dione Chemical compound O=C1CC(=O)C=CN1 UUDALWDRIFYZPM-UHFFFAOYSA-N 0.000 claims 1
- UUKIBUXWKXFKLI-UHFFFAOYSA-N 3-[[1-[(2-chlorophenyl)methyl]-4-hydroxy-2-oxopyridin-3-yl]carbamoylamino]-3-naphthalen-2-ylpropanoic acid Chemical compound C=1C=C2C=CC=CC2=CC=1C(CC(=O)O)NC(=O)NC(C1=O)=C(O)C=CN1CC1=CC=CC=C1Cl UUKIBUXWKXFKLI-UHFFFAOYSA-N 0.000 claims 1
- JGSIAOZAXBWRFO-UHFFFAOYSA-N 3-methylsulfanyl-1-phenyl-4,5-dihydrobenzo[g]indazole Chemical compound C1CC2=CC=CC=C2C2=C1C(SC)=NN2C1=CC=CC=C1 JGSIAOZAXBWRFO-UHFFFAOYSA-N 0.000 claims 1
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- REEHGJBMJSCWRI-UHFFFAOYSA-N 5-[(2,4-dichlorophenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound ClC1=CC(Cl)=CC=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 REEHGJBMJSCWRI-UHFFFAOYSA-N 0.000 claims 1
- HSMUOJYMOIPMJH-UHFFFAOYSA-N 5-[(2,4-dichlorophenyl)methyl]-7-methyl-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound O=C1C=2NC(=O)OC=2C(C)=CN1CC1=CC=C(Cl)C=C1Cl HSMUOJYMOIPMJH-UHFFFAOYSA-N 0.000 claims 1
- CLNHGKWUXLAOOJ-UHFFFAOYSA-N 5-[(2,4-difluorophenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound FC1=CC(F)=CC=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 CLNHGKWUXLAOOJ-UHFFFAOYSA-N 0.000 claims 1
- XMHISXICUBQNMC-UHFFFAOYSA-N 5-[(2,5-difluorophenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound FC1=CC=C(F)C(CN2C(C=3NC(=O)OC=3C=C2)=O)=C1 XMHISXICUBQNMC-UHFFFAOYSA-N 0.000 claims 1
- JHQDBUNUHQTXIF-UHFFFAOYSA-N 5-[(2,5-dimethylphenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound CC1=CC=C(C)C(CN2C(C=3NC(=O)OC=3C=C2)=O)=C1 JHQDBUNUHQTXIF-UHFFFAOYSA-N 0.000 claims 1
- ZXQAFRNZBLKLCH-UHFFFAOYSA-N 5-[(2,6-dichlorophenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound ClC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 ZXQAFRNZBLKLCH-UHFFFAOYSA-N 0.000 claims 1
- YCROZHHKJRMEQY-UHFFFAOYSA-N 5-[(2,6-difluorophenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound FC1=CC=CC(F)=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 YCROZHHKJRMEQY-UHFFFAOYSA-N 0.000 claims 1
- SQOZHBVFGLKGRE-UHFFFAOYSA-N 5-[(2-bromophenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound BrC1=CC=CC=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 SQOZHBVFGLKGRE-UHFFFAOYSA-N 0.000 claims 1
- YXEMIQIKYBDOTJ-UHFFFAOYSA-N 5-[(2-chloro-5-fluorophenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound FC1=CC=C(Cl)C(CN2C(C=3NC(=O)OC=3C=C2)=O)=C1 YXEMIQIKYBDOTJ-UHFFFAOYSA-N 0.000 claims 1
- QDMAGZQORXHWRQ-UHFFFAOYSA-N 5-[(2-chloro-5-fluorophenyl)methyl]-7-methyl-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound O=C1C=2NC(=O)OC=2C(C)=CN1CC1=CC(F)=CC=C1Cl QDMAGZQORXHWRQ-UHFFFAOYSA-N 0.000 claims 1
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- JWHHZPCJWPFOAV-UHFFFAOYSA-N 5-[(2-chloro-6-methoxyphenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound COC1=CC=CC(Cl)=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 JWHHZPCJWPFOAV-UHFFFAOYSA-N 0.000 claims 1
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- JOXFCWDMVPBRNO-UHFFFAOYSA-N 5-[(4-chlorophenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound C1=CC(Cl)=CC=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 JOXFCWDMVPBRNO-UHFFFAOYSA-N 0.000 claims 1
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- MFJSYLJZTRGLPN-UHFFFAOYSA-N 5-[(4-fluorophenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound C1=CC(F)=CC=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 MFJSYLJZTRGLPN-UHFFFAOYSA-N 0.000 claims 1
- BIIJKUZXXWVKGA-UHFFFAOYSA-N 5-[(4-methylphenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound C1=CC(C)=CC=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 BIIJKUZXXWVKGA-UHFFFAOYSA-N 0.000 claims 1
- LMXGXFQJWWQXOK-UHFFFAOYSA-N 5-[(4-tert-butylphenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound C1=CC(C(C)(C)C)=CC=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 LMXGXFQJWWQXOK-UHFFFAOYSA-N 0.000 claims 1
- SJWCLIPUIRSJFR-UHFFFAOYSA-N 5-[[2-(trifluoromethyl)phenyl]methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound FC(F)(F)C1=CC=CC=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 SJWCLIPUIRSJFR-UHFFFAOYSA-N 0.000 claims 1
- YTSHFBSPGHCIDH-UHFFFAOYSA-N 5-[[2-chloro-5-(trifluoromethyl)phenyl]methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound FC(F)(F)C1=CC=C(Cl)C(CN2C(C=3NC(=O)OC=3C=C2)=O)=C1 YTSHFBSPGHCIDH-UHFFFAOYSA-N 0.000 claims 1
- FGDMQKJXXJGDDK-UHFFFAOYSA-N 5-[[2-chloro-5-(trifluoromethyl)phenyl]methyl]-7-methyl-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound O=C1C=2NC(=O)OC=2C(C)=CN1CC1=CC(C(F)(F)F)=CC=C1Cl FGDMQKJXXJGDDK-UHFFFAOYSA-N 0.000 claims 1
- LYGUPGQILLFCDY-UHFFFAOYSA-N 5-[[2-chloro-6-(cyclopentylmethoxy)phenyl]methyl]-7-methyl-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound O=C1C=2NC(=O)OC=2C(C)=CN1CC1=C(Cl)C=CC=C1OCC1CCCC1 LYGUPGQILLFCDY-UHFFFAOYSA-N 0.000 claims 1
- FCTXOZKZNMRGDL-UHFFFAOYSA-N 5-[[3,5-bis(trifluoromethyl)phenyl]methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound FC(F)(F)C1=CC(C(F)(F)F)=CC(CN2C(C=3NC(=O)OC=3C=C2)=O)=C1 FCTXOZKZNMRGDL-UHFFFAOYSA-N 0.000 claims 1
- IHMJUNFHKBBHSS-UHFFFAOYSA-N 5-[[3-(trifluoromethyl)phenyl]methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound FC(F)(F)C1=CC=CC(CN2C(C=3NC(=O)OC=3C=C2)=O)=C1 IHMJUNFHKBBHSS-UHFFFAOYSA-N 0.000 claims 1
- CNXNHKAIHFVUDT-UHFFFAOYSA-N 5-[[4-(trifluoromethoxy)phenyl]methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound C1=CC(OC(F)(F)F)=CC=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 CNXNHKAIHFVUDT-UHFFFAOYSA-N 0.000 claims 1
- VJIMPARYEDYYSX-UHFFFAOYSA-N 5-[[4-(trifluoromethyl)phenyl]methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound C1=CC(C(F)(F)F)=CC=C1CN1C(=O)C(NC(=O)O2)=C2C=C1 VJIMPARYEDYYSX-UHFFFAOYSA-N 0.000 claims 1
- NGLSRQWOZPGYCA-UHFFFAOYSA-N 5-benzyl-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound O1C(=O)NC(C2=O)=C1C=CN2CC1=CC=CC=C1 NGLSRQWOZPGYCA-UHFFFAOYSA-N 0.000 claims 1
- PENMOQZDNRRAQK-UHFFFAOYSA-N 5-benzyl-6-methyl-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound CC1=CC=2OC(=O)NC=2C(=O)N1CC1=CC=CC=C1 PENMOQZDNRRAQK-UHFFFAOYSA-N 0.000 claims 1
- MJQAAEHTCMTXQL-UHFFFAOYSA-N 7-butyl-5-[(2-chlorophenyl)methyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound O=C1C=2NC(=O)OC=2C(CCCC)=CN1CC1=CC=CC=C1Cl MJQAAEHTCMTXQL-UHFFFAOYSA-N 0.000 claims 1
- OUQDWMSQLUOELS-JTQLQIEISA-N 7-methyl-5-[(1s)-1-phenylethyl]-3h-[1,3]oxazolo[4,5-c]pyridine-2,4-dione Chemical compound C1([C@H](C)N2C(C=3NC(=O)OC=3C(C)=C2)=O)=CC=CC=C1 OUQDWMSQLUOELS-JTQLQIEISA-N 0.000 claims 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
- 239000005711 Benzoic acid Substances 0.000 claims 1
- QAICGVDFJBCANR-UHFFFAOYSA-N CCOC1=CC=C(Cl)C(Cl)=C1CN1C(=O)C(NC(=O)O2)=C2C2=C1CCC2 Chemical compound CCOC1=CC=C(Cl)C(Cl)=C1CN1C(=O)C(NC(=O)O2)=C2C2=C1CCC2 QAICGVDFJBCANR-UHFFFAOYSA-N 0.000 claims 1
- PBMWKSYVBJRLHO-UHFFFAOYSA-N ClC1=CC=CC=C1CN1C(=O)C(NC(=O)O2)=C2C2=C1CCC2 Chemical compound ClC1=CC=CC=C1CN1C(=O)C(NC(=O)O2)=C2C2=C1CCC2 PBMWKSYVBJRLHO-UHFFFAOYSA-N 0.000 claims 1
- 241001024304 Mino Species 0.000 claims 1
- 229910006074 SO2NH2 Inorganic materials 0.000 claims 1
- 229910006069 SO3H Inorganic materials 0.000 claims 1
- VXZXLBBZGYELLZ-UHFFFAOYSA-N [1,3]oxazolo[4,5-c]quinoline-2,4-dione Chemical compound O1C(N=C2C(N=C3C=CC=CC3=C21)=O)=O VXZXLBBZGYELLZ-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 1
- 235000010233 benzoic acid Nutrition 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000003831 tetrazolyl group Chemical group 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 1
- 108010000134 Vascular Cell Adhesion Molecule-1 Proteins 0.000 abstract 2
- 102100023543 Vascular cell adhesion protein 1 Human genes 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 102000016359 Fibronectins Human genes 0.000 abstract 1
- 108010067306 Fibronectins Proteins 0.000 abstract 1
- 230000006806 disease prevention Effects 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 0 CC(C(C*)*1CC(C=CC)=C*)(C(ONOC*2*)=C2C1=O)O Chemical compound CC(C(C*)*1CC(C=CC)=C*)(C(ONOC*2*)=C2C1=O)O 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—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
- 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
- C07D213/60—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 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—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
- 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
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
- C07D221/06—Ring systems of three rings
- C07D221/16—Ring systems of three rings containing carbocyclic rings other than six-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three 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
- C07D237/22—Nitrogen and oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
- C07D317/60—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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- C—CHEMISTRY; METALLURGY
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
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| US09/973,142 | 2001-10-09 | ||
| US09/973,142 US6972296B2 (en) | 1999-05-07 | 2001-10-09 | Carboxylic acid derivatives that inhibit the binding of integrins to their receptors |
Publications (2)
| Publication Number | Publication Date |
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| CA2366800A1 true CA2366800A1 (fr) | 2003-04-10 |
| CA2366800C CA2366800C (fr) | 2010-08-10 |
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| CA 2366800 Expired - Fee Related CA2366800C (fr) | 2001-10-09 | 2002-01-07 | Derives de l'acide carboxylique qui inhibent la liaison d'integrines a leurs recepteurs |
Country Status (6)
| Country | Link |
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| JP (1) | JP4149172B2 (fr) |
| CN (2) | CN101475526B (fr) |
| CA (1) | CA2366800C (fr) |
| PL (1) | PL223151B1 (fr) |
| SG (2) | SG107574A1 (fr) |
| SI (1) | SI21096B (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008109991A1 (fr) * | 2007-03-09 | 2008-09-18 | University Health Network | Inhibiteur de carnitine palmitoyltransférase et traitement du cancer |
| US8680282B2 (en) | 2007-08-01 | 2014-03-25 | University Health Network | Cyclic inhibitors of carnitine palmitoyltransferase and treating cancer |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ539790A (en) * | 2002-11-08 | 2007-09-28 | Schering Corp | Combination products with carboxylic acid derivatives that inhibit the binding of integrins to their receptors and other therapeutic compounds |
| WO2010126914A1 (fr) * | 2009-04-27 | 2010-11-04 | Elan Pharmaceuticals, Inc. | Antagonistes à base de pyridinone d'intégrines alpha-4 |
| US10875875B2 (en) * | 2017-04-26 | 2020-12-29 | Aviara Pharmaceuticals, Inc. | Propionic acid derivatives and methods of use thereof |
| CN118591535A (zh) * | 2021-12-27 | 2024-09-03 | 西藏海思科制药有限公司 | 一种丙酸衍生物及其在医药上的应用 |
| TW202416966A (zh) * | 2022-09-09 | 2024-05-01 | 大陸商西藏海思科製藥有限公司 | 丙酸衍生物及其在醫藥上的應用 |
| WO2025124544A1 (fr) * | 2023-12-14 | 2025-06-19 | 华润医药研究院(深圳)有限公司 | Composé 3,4-dihydro-2h-benzo[b][1,4]dioxépane, et son procédé de préparation et son utilisation pharmaceutique |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2614189A1 (de) * | 1976-04-02 | 1977-10-20 | Hoechst Ag | Therapeutisch wirksame ureido- und semicarbazido-derivate des tiazols und verfahren zu ihrer herstellung |
| WO1990002112A1 (fr) * | 1988-08-23 | 1990-03-08 | The Nutrasweet Company | Arylurees substituees utilisees comme edulcorants de forte puissance |
| FR2659653B1 (fr) * | 1990-03-13 | 1992-05-22 | Rhone Poulenc Sante | Derives de l'uree, leur preparation et les medicaments les contenant. |
| WO1992019595A1 (fr) * | 1991-05-07 | 1992-11-12 | Merck & Co., Inc. | Antagonistes de recepteur de fibrinogene |
| EP0691953B1 (fr) * | 1993-03-31 | 2000-08-02 | G.D. Searle & Co. | Amidinophenyl-1-pyrrolidones /piperidinones inhibitrices de l'agregation plaquettaire |
| US5610296A (en) * | 1994-12-05 | 1997-03-11 | G. D. Searle & Co. | Process for the preparation of amidino phenyl pyrrolidine beta-alanine urea analogs |
| IL138973A0 (en) * | 1998-04-16 | 2001-11-25 | Texas Biotechnology Corp | Compounds that inhibit the binding of integrins to their receptors |
| ATE383153T1 (de) * | 1999-05-07 | 2008-01-15 | Encysive Pharmaceuticals Inc | Carbonsäurederivate die die bindung von integrinen an ihre rezeptoren hemmen |
-
2001
- 2001-11-05 SI SI200100288A patent/SI21096B/sl active Search and Examination
- 2001-12-29 CN CN2009100098615A patent/CN101475526B/zh not_active Expired - Fee Related
- 2001-12-29 CN CNB011451823A patent/CN100491353C/zh not_active Expired - Fee Related
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2002
- 2002-01-07 CA CA 2366800 patent/CA2366800C/fr not_active Expired - Fee Related
- 2002-01-16 SG SG200200313A patent/SG107574A1/en unknown
- 2002-01-16 SG SG200604940-7A patent/SG161741A1/en unknown
- 2002-02-08 JP JP2002031953A patent/JP4149172B2/ja not_active Expired - Fee Related
- 2002-10-08 PL PL356532A patent/PL223151B1/pl unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008109991A1 (fr) * | 2007-03-09 | 2008-09-18 | University Health Network | Inhibiteur de carnitine palmitoyltransférase et traitement du cancer |
| US8410150B2 (en) | 2007-03-09 | 2013-04-02 | University Health Network | Inhibitors of carnitine palmitoyltransferase and treating cancer |
| US8680282B2 (en) | 2007-08-01 | 2014-03-25 | University Health Network | Cyclic inhibitors of carnitine palmitoyltransferase and treating cancer |
Also Published As
| Publication number | Publication date |
|---|---|
| SI21096B (sl) | 2012-05-31 |
| PL356532A1 (en) | 2003-04-22 |
| CA2366800C (fr) | 2010-08-10 |
| CN100491353C (zh) | 2009-05-27 |
| SG161741A1 (en) | 2010-06-29 |
| CN101475526B (zh) | 2011-05-25 |
| CN1412181A (zh) | 2003-04-23 |
| CN101475526A (zh) | 2009-07-08 |
| JP4149172B2 (ja) | 2008-09-10 |
| PL223151B1 (pl) | 2016-10-31 |
| SI21096A1 (sl) | 2003-06-30 |
| SG107574A1 (en) | 2004-12-29 |
| JP2003119181A (ja) | 2003-04-23 |
| HK1135376A1 (en) | 2010-06-04 |
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