JP2010515733A5 - - Google Patents
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- JP2010515733A5 JP2010515733A5 JP2009545577A JP2009545577A JP2010515733A5 JP 2010515733 A5 JP2010515733 A5 JP 2010515733A5 JP 2009545577 A JP2009545577 A JP 2009545577A JP 2009545577 A JP2009545577 A JP 2009545577A JP 2010515733 A5 JP2010515733 A5 JP 2010515733A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbonyl
- alkyl
- cyclo
- chroman
- 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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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 78
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 36
- 125000005843 halogen group Chemical group 0.000 claims 35
- 125000006828 (C2-C7) alkoxycarbonyl group Chemical group 0.000 claims 27
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 23
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 23
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 22
- 125000001424 substituent group Chemical group 0.000 claims 21
- 150000002148 esters Chemical class 0.000 claims 19
- 150000003839 salts Chemical class 0.000 claims 19
- 125000003545 alkoxy group Chemical group 0.000 claims 17
- 125000002252 acyl group Chemical group 0.000 claims 16
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 15
- 125000003118 aryl group Chemical group 0.000 claims 13
- 125000004043 oxo group Chemical group O=* 0.000 claims 13
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 12
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 11
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 10
- 125000004414 alkyl thio group Chemical group 0.000 claims 10
- 125000000623 heterocyclic group Chemical group 0.000 claims 10
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 8
- 125000004430 oxygen atom Chemical group O* 0.000 claims 8
- 229910052717 sulfur Inorganic materials 0.000 claims 8
- 125000004434 sulfur atom Chemical group 0.000 claims 8
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 7
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 7
- 125000000464 thioxo group Chemical group S=* 0.000 claims 7
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 6
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 claims 6
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 claims 6
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims 6
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 6
- -1 1-Ethyl-4-methoxy-1H-benzimidazol-6-yl Chemical group 0.000 claims 5
- 125000004423 acyloxy group Chemical group 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- KTZQTRPPVKQPFO-UHFFFAOYSA-N 1,2-benzoxazole Chemical compound C1=CC=C2C=NOC2=C1 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 claims 3
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 claims 3
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims 3
- GVLRTOYGRNLSDW-UHFFFAOYSA-N 1h-pyrazolo[3,4-b]pyridine Chemical compound C1=CC=C2C=NNC2=N1 GVLRTOYGRNLSDW-UHFFFAOYSA-N 0.000 claims 3
- FKWUPVHNVKGGSD-UHFFFAOYSA-N 1h-thieno[2,3-c]pyrazole Chemical compound C1=NNC2=C1C=CS2 FKWUPVHNVKGGSD-UHFFFAOYSA-N 0.000 claims 3
- 125000002947 alkylene group Chemical group 0.000 claims 3
- KZOWNALBTMILAP-JBMRGDGGSA-N ancitabine hydrochloride Chemical compound Cl.N=C1C=CN2[C@@H]3O[C@H](CO)[C@@H](O)[C@@H]3OC2=N1 KZOWNALBTMILAP-JBMRGDGGSA-N 0.000 claims 3
- 125000005098 aryl alkoxy carbonyl group Chemical group 0.000 claims 3
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims 3
- IVRMZWNICZWHMI-UHFFFAOYSA-N azide group Chemical group [N-]=[N+]=[N-] IVRMZWNICZWHMI-UHFFFAOYSA-N 0.000 claims 3
- UTCSSFWDNNEEBH-UHFFFAOYSA-N imidazo[1,2-a]pyridine Chemical compound C1=CC=CC2=NC=CN21 UTCSSFWDNNEEBH-UHFFFAOYSA-N 0.000 claims 3
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims 3
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- 125000003831 tetrazolyl group Chemical group 0.000 claims 3
- 208000032841 Bulimia Diseases 0.000 claims 2
- 206010006550 Bulimia nervosa Diseases 0.000 claims 2
- 208000035473 Communicable disease Diseases 0.000 claims 2
- 208000004930 Fatty Liver Diseases 0.000 claims 2
- 206010019708 Hepatic steatosis Diseases 0.000 claims 2
- 208000031226 Hyperlipidaemia Diseases 0.000 claims 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 2
- 208000001145 Metabolic Syndrome Diseases 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 208000008589 Obesity Diseases 0.000 claims 2
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 206010012601 diabetes mellitus Diseases 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 208000010706 fatty liver disease Diseases 0.000 claims 2
- 208000015181 infectious disease Diseases 0.000 claims 2
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 235000020824 obesity Nutrition 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims 2
- 239000011734 sodium Substances 0.000 claims 2
- 229910052708 sodium Inorganic materials 0.000 claims 2
- 231100000240 steatosis hepatitis Toxicity 0.000 claims 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- OEOFWVOLIASGRM-UHFFFAOYSA-N (1-cyclopropyl-4-methoxyindol-6-yl)-[6-(2H-tetrazol-5-yl)spiro[3,4-dihydrochromene-2,4'-piperidine]-1'-yl]methanone Chemical compound C1(CC1)N1C=CC2=C(C=C(C=C12)C(=O)N1CCC2(CC1)OC1=CC=C(C=C1CC2)C1=NN=NN1)OC OEOFWVOLIASGRM-UHFFFAOYSA-N 0.000 claims 1
- 125000006773 (C2-C7) alkylcarbonyl group Chemical group 0.000 claims 1
- SEPPVOUBHWNCAW-FNORWQNLSA-N (E)-4-oxonon-2-enal Chemical compound CCCCCC(=O)\C=C\C=O SEPPVOUBHWNCAW-FNORWQNLSA-N 0.000 claims 1
- AWNDPNWXFGRJQI-UHFFFAOYSA-N 1'-(1,3-diethyl-7-methoxy-2-oxobenzimidazole-5-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C=1C(OC)=C2N(CC)C(=O)N(CC)C2=CC=1C(=O)N(CC1)CCC1(OC1=CC=2)CC(=O)C1=CC=2C1=NN=NN1 AWNDPNWXFGRJQI-UHFFFAOYSA-N 0.000 claims 1
- JHWHHWDHRLPXLG-UHFFFAOYSA-N 1'-(1,4-diethoxyindazole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C=1C=2N(OCC)N=CC=2C(OCC)=CC=1C(=O)N(CC1)CCC1(OC1=CC=2)CC(=O)C1=CC=2C1=NN=NN1 JHWHHWDHRLPXLG-UHFFFAOYSA-N 0.000 claims 1
- OAMOWQJTVYLHGK-UHFFFAOYSA-N 1'-(1,4-dimethoxyindole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C=1C=2N(OC)C=CC=2C(OC)=CC=1C(=O)N(CC1)CCC1(OC1=CC=2)CC(=O)C1=CC=2C1=NN=NN1 OAMOWQJTVYLHGK-UHFFFAOYSA-N 0.000 claims 1
- YPJUVNXGAKFASN-UHFFFAOYSA-N 1'-(1,4-dimethoxyindole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one;sodium Chemical compound [Na].C=1C=2N(OC)C=CC=2C(OC)=CC=1C(=O)N(CC1)CCC1(OC1=CC=2)CC(=O)C1=CC=2C=1N=NNN=1 YPJUVNXGAKFASN-UHFFFAOYSA-N 0.000 claims 1
- JFAWMIWDSQSOMV-UHFFFAOYSA-N 1'-(1-cyclopropyl-4-ethoxy-3-methylindole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=C(C)C=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2N1C1CC1 JFAWMIWDSQSOMV-UHFFFAOYSA-N 0.000 claims 1
- LPWKEJNQEJOLNF-UHFFFAOYSA-N 1'-(1-cyclopropyl-4-ethoxyindole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=CC=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2N1C1CC1 LPWKEJNQEJOLNF-UHFFFAOYSA-N 0.000 claims 1
- OJQNMRDPSKTWSY-UHFFFAOYSA-N 1'-(1-cyclopropyl-4-ethoxyindole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one;sodium Chemical compound [Na].C1=CC=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C3=NNN=N3)=CC=2N1C1CC1 OJQNMRDPSKTWSY-UHFFFAOYSA-N 0.000 claims 1
- MWOXXNTYIFYXJQ-UHFFFAOYSA-N 1'-(1-cyclopropyl-4-methoxy-3-methylindole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=C(C)C=2C(OC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2N1C1CC1 MWOXXNTYIFYXJQ-UHFFFAOYSA-N 0.000 claims 1
- JQKVGZANRSXPOU-UHFFFAOYSA-N 1'-(1-cyclopropyl-4-methoxyindole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=CC=2C(OC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2N1C1CC1 JQKVGZANRSXPOU-UHFFFAOYSA-N 0.000 claims 1
- DZCHXXJDTKQUOA-UHFFFAOYSA-N 1'-(1-cyclopropyl-4-methoxyindole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one;sodium Chemical compound [Na].C1=CC=2C(OC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C3=NNN=N3)=CC=2N1C1CC1 DZCHXXJDTKQUOA-UHFFFAOYSA-N 0.000 claims 1
- AJUCBKYSAOERCP-UHFFFAOYSA-N 1'-(1-cyclopropyl-4-methoxyindole-6-carbonyl)-6-(5-oxo-1,2-dihydro-1,2,4-triazol-3-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=CC=2C(OC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NC(=O)NN=3)=CC=2N1C1CC1 AJUCBKYSAOERCP-UHFFFAOYSA-N 0.000 claims 1
- VXOXUMFIISPGSV-UHFFFAOYSA-N 1'-(1-cyclopropyl-4-methoxyindole-6-carbonyl)-6-(5-oxo-2h-1,2,4-oxadiazol-3-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=CC=2C(OC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NC(=O)ON=3)=CC=2N1C1CC1 VXOXUMFIISPGSV-UHFFFAOYSA-N 0.000 claims 1
- OYZMUGLPMDQPDV-UHFFFAOYSA-N 1'-(1-ethyl-3-methylthieno[2,3-c]pyrazole-5-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound S1C=2N(CC)N=C(C)C=2C=C1C(=O)N(CC1)CCC1(OC1=CC=2)CC(=O)C1=CC=2C1=NN=NN1 OYZMUGLPMDQPDV-UHFFFAOYSA-N 0.000 claims 1
- NKDMEHKUJITRJR-UHFFFAOYSA-N 1'-(1-ethyl-4-methoxyindazole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=C2N(CC)N=CC2=C(OC)C=C1C(=O)N(CC1)CCC1(OC1=CC=2)CC(=O)C1=CC=2C1=NN=NN1 NKDMEHKUJITRJR-UHFFFAOYSA-N 0.000 claims 1
- ZMELGQVAMKHNGD-UHFFFAOYSA-N 1'-(1-ethyl-4-methoxyindole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=C2N(CC)C=CC2=C(OC)C=C1C(=O)N(CC1)CCC1(OC1=CC=2)CC(=O)C1=CC=2C1=NN=NN1 ZMELGQVAMKHNGD-UHFFFAOYSA-N 0.000 claims 1
- AWKUNWUUMKOYCI-UHFFFAOYSA-N 1'-(1-ethyl-4-morpholin-4-ylindole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=C2N(CC)C=CC2=C(N2CCOCC2)C=C1C(=O)N(CC1)CCC1(OC1=CC=2)CC(=O)C1=CC=2C1=NN=NN1 AWKUNWUUMKOYCI-UHFFFAOYSA-N 0.000 claims 1
- BQDDEWPJPSWXRR-UHFFFAOYSA-N 1'-(2-cyclopropyl-7-ethoxy-1,3-benzoxazole-5-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound O1C=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2N=C1C1CC1 BQDDEWPJPSWXRR-UHFFFAOYSA-N 0.000 claims 1
- XUYLEIKOZAMWOE-UHFFFAOYSA-N 1'-(3-chloro-1-cyclopropyl-4-ethoxyindole-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=C(Cl)C=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2N1C1CC1 XUYLEIKOZAMWOE-UHFFFAOYSA-N 0.000 claims 1
- OCRONEAVJHGACD-UHFFFAOYSA-N 1'-(3-chloro-1-cyclopropyl-7-ethoxyindole-5-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2C(Cl)=CN1C1CC1 OCRONEAVJHGACD-UHFFFAOYSA-N 0.000 claims 1
- ZLDRXVSQRSQAOV-UHFFFAOYSA-N 1'-(3-cyclopropyl-7-ethoxy-1,2-benzoxazole-5-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound N=1OC=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2C=1C1CC1 ZLDRXVSQRSQAOV-UHFFFAOYSA-N 0.000 claims 1
- JHCULCUEXUZDTM-UHFFFAOYSA-N 1'-(3-cyclopropyl-7-methoxybenzimidazole-5-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=NC=2C(OC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2N1C1CC1 JHCULCUEXUZDTM-UHFFFAOYSA-N 0.000 claims 1
- GKXFKKPTSSQZNU-UHFFFAOYSA-N 1'-(3-cyclopropyl-8-methoxyimidazo[1,2-a]pyridine-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C=1N=C2C(OC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CN2C=1C1CC1 GKXFKKPTSSQZNU-UHFFFAOYSA-N 0.000 claims 1
- AFKBHASOWVCPBV-UHFFFAOYSA-N 1'-(4-acetyl-7-methoxy-1-benzofuran-2-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound O1C=2C(OC)=CC=C(C(C)=O)C=2C=C1C(=O)N(CC1)CCC1(OC1=CC=2)CC(=O)C1=CC=2C1=NN=NN1 AFKBHASOWVCPBV-UHFFFAOYSA-N 0.000 claims 1
- OQZSPIHVLNEMOM-UHFFFAOYSA-N 1'-(4-methoxy-1-methylpyrazolo[3,4-b]pyridine-6-carbonyl)-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound N=1C=2N(C)N=CC=2C(OC)=CC=1C(=O)N(CC1)CCC1(OC1=CC=2)CC(=O)C1=CC=2C1=NN=NN1 OQZSPIHVLNEMOM-UHFFFAOYSA-N 0.000 claims 1
- YWEBYUIRXNXPKJ-UHFFFAOYSA-N 1'-[1-cyclopropyl-4-(2-hydroxyethoxy)indole-6-carbonyl]-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=CC=2C(OCCO)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2N1C1CC1 YWEBYUIRXNXPKJ-UHFFFAOYSA-N 0.000 claims 1
- VIINMHDSRKGUSP-UHFFFAOYSA-N 1'-[1-ethyl-4-(2-hydroxyethoxy)indole-6-carbonyl]-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-4-one Chemical compound C1=C2N(CC)C=CC2=C(OCCO)C=C1C(=O)N(CC1)CCC1(OC1=CC=2)CC(=O)C1=CC=2C1=NN=NN1 VIINMHDSRKGUSP-UHFFFAOYSA-N 0.000 claims 1
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims 1
- MMOGEKMWSXYDNU-UHFFFAOYSA-N 1-cyclopropyl-4-ethoxy-6-[4-oxo-6-(1h-pyrazol-4-yl)spiro[3h-chromene-2,4'-piperidine]-1'-carbonyl]indole-3-carboxylic acid Chemical compound C1=C(C(O)=O)C=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C3=CNN=C3)=CC=2N1C1CC1 MMOGEKMWSXYDNU-UHFFFAOYSA-N 0.000 claims 1
- VYYLYKNBTKXAJC-UHFFFAOYSA-N 1-cyclopropyl-4-ethoxy-6-[4-oxo-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-1'-carbonyl]indole-3-carboxamide Chemical compound C1=C(C(N)=O)C=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2N1C1CC1 VYYLYKNBTKXAJC-UHFFFAOYSA-N 0.000 claims 1
- BPNDISJEGZBLQJ-UHFFFAOYSA-N 1-cyclopropyl-4-ethoxy-6-[6-[(2-methylpyrazol-3-yl)amino]-4-oxospiro[3h-chromene-2,4'-piperidine]-1'-carbonyl]indole-3-carboxylic acid Chemical compound C1=C(C(O)=O)C=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(NC=5N(N=CC=5)C)C=C3C(=O)C4)=CC=2N1C1CC1 BPNDISJEGZBLQJ-UHFFFAOYSA-N 0.000 claims 1
- WTFVNBJKZFCVHC-UHFFFAOYSA-N 1-cyclopropyl-4-ethoxy-n-methyl-6-[4-oxo-6-(2h-tetrazol-5-yl)spiro[3h-chromene-2,4'-piperidine]-1'-carbonyl]indole-3-carboxamide Chemical compound C1=C(C(=O)NC)C=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NN=NN=3)=CC=2N1C1CC1 WTFVNBJKZFCVHC-UHFFFAOYSA-N 0.000 claims 1
- USCXFVCAIMZLJL-UHFFFAOYSA-N 3-[1'-(1-cyclopropyl-4-methoxyindole-6-carbonyl)-4-oxospiro[3h-chromene-2,4'-piperidine]-6-yl]-1h-1,2,4-triazole-5-carboxamide Chemical compound C1=CC=2C(OC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3NC(=NN=3)C(N)=O)=CC=2N1C1CC1 USCXFVCAIMZLJL-UHFFFAOYSA-N 0.000 claims 1
- PDAJKOILZCBVGF-UHFFFAOYSA-N 3-[1'-(1-cyclopropyl-4-methoxyindole-6-carbonyl)-4-oxospiro[3h-chromene-2,4'-piperidine]-6-yl]benzoic acid Chemical compound C1=CC=2C(OC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3C=C(C=CC=3)C(O)=O)=CC=2N1C1CC1 PDAJKOILZCBVGF-UHFFFAOYSA-N 0.000 claims 1
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- LLBZPESJRQGYMB-UHFFFAOYSA-N 4-one Natural products O1C(C(=O)CC)CC(C)C11C2(C)CCC(C3(C)C(C(C)(CO)C(OC4C(C(O)C(O)C(COC5C(C(O)C(O)CO5)OC5C(C(OC6C(C(O)C(O)C(CO)O6)O)C(O)C(CO)O5)OC5C(C(O)C(O)C(C)O5)O)O4)O)CC3)CC3)=C3C2(C)CC1 LLBZPESJRQGYMB-UHFFFAOYSA-N 0.000 claims 1
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- APPNDGWGOXONSC-UHFFFAOYSA-N 5-[1'-(1-cyclopropyl-4-ethoxy-3-methylindole-6-carbonyl)-4-oxospiro[3h-chromene-2,4'-piperidine]-6-yl]-2-methylpyridine-3-carboxylic acid Chemical group C1=C(C)C=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3C=C(C(C)=NC=3)C(O)=O)=CC=2N1C1CC1 APPNDGWGOXONSC-UHFFFAOYSA-N 0.000 claims 1
- WFWSTFMGVNHXSR-UHFFFAOYSA-N 5-[1'-(1-cyclopropyl-4-ethoxy-3-methylindole-6-carbonyl)-4-oxospiro[3h-chromene-2,4'-piperidine]-6-yl]pyridine-3-carboxylic acid Chemical compound C1=C(C)C=2C(OCC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3C=C(C=NC=3)C(O)=O)=CC=2N1C1CC1 WFWSTFMGVNHXSR-UHFFFAOYSA-N 0.000 claims 1
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- WDBNGXLHMZSUEI-UHFFFAOYSA-N 5-[1'-(1-cyclopropyl-4-methoxy-3-methylindole-6-carbonyl)-4-oxospiro[3h-chromene-2,4'-piperidine]-6-yl]pyridine-3-carboxylic acid Chemical compound C1=C(C)C=2C(OC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3C=C(C=NC=3)C(O)=O)=CC=2N1C1CC1 WDBNGXLHMZSUEI-UHFFFAOYSA-N 0.000 claims 1
- JOIYYAUZXKGMEN-UHFFFAOYSA-N 5-[1'-(1-cyclopropyl-4-methoxyindole-6-carbonyl)-4-oxospiro[3h-chromene-2,4'-piperidine]-6-yl]pyridine-3-carboxylic acid Chemical compound C1=CC=2C(OC)=CC(C(=O)N3CCC4(CC3)OC3=CC=C(C=C3C(=O)C4)C=3C=C(C=NC=3)C(O)=O)=CC=2N1C1CC1 JOIYYAUZXKGMEN-UHFFFAOYSA-N 0.000 claims 1
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-
2008
- 2008-01-04 PE PE2008000089A patent/PE20081559A1/es not_active Application Discontinuation
- 2008-01-07 TW TW097100608A patent/TW200836727A/zh unknown
- 2008-01-08 KR KR1020097014377A patent/KR20090108022A/ko not_active Withdrawn
- 2008-01-08 WO PCT/US2008/000223 patent/WO2008088689A1/en not_active Ceased
- 2008-01-08 BR BRPI0806531-4A2A patent/BRPI0806531A2/pt not_active IP Right Cessation
- 2008-01-08 CN CN2008800021443A patent/CN101631791B/zh not_active Expired - Fee Related
- 2008-01-08 EP EP08713050A patent/EP2111406B1/en active Active
- 2008-01-08 CA CA2674573A patent/CA2674573C/en not_active Expired - Fee Related
- 2008-01-08 SG SG2012002739A patent/SG177977A1/en unknown
- 2008-01-08 AU AU2008205638A patent/AU2008205638B2/en not_active Ceased
- 2008-01-08 MX MX2009007502A patent/MX2009007502A/es unknown
- 2008-01-08 WO PCT/US2008/000221 patent/WO2008088688A1/en not_active Ceased
- 2008-01-08 RU RU2009130736/04A patent/RU2009130736A/ru not_active Application Discontinuation
- 2008-01-08 UA UAA200908468A patent/UA103990C2/ru unknown
- 2008-01-08 NZ NZ577825A patent/NZ577825A/en not_active IP Right Cessation
- 2008-01-08 JP JP2009545577A patent/JP5319550B2/ja not_active Expired - Fee Related
- 2008-01-08 US US12/007,000 patent/US8093389B2/en active Active
- 2008-01-09 AR ARP080100081A patent/AR064824A1/es not_active Application Discontinuation
- 2008-01-10 CL CL200800067A patent/CL2008000067A1/es unknown
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2009
- 2009-06-12 ZA ZA200904138A patent/ZA200904138B/xx unknown
- 2009-07-06 GT GT200900194A patent/GT200900194A/es unknown
- 2009-07-06 HN HN2009001276A patent/HN2009001276A/es unknown
- 2009-07-08 NI NI200900139A patent/NI200900139A/es unknown
- 2009-07-09 EC EC2009009503A patent/ECSP099503A/es unknown
- 2009-07-09 DO DO2009000176A patent/DOP2009000176A/es unknown
- 2009-07-13 CO CO09072490A patent/CO6190611A2/es active IP Right Grant
- 2009-07-20 CR CR10944A patent/CR10944A/es unknown
- 2009-07-23 MA MA32114A patent/MA31108B1/fr unknown
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