JP5268912B2 - 環状11−βヒドロキシステロイドデヒドロゲナーゼI型阻害剤 - Google Patents
環状11−βヒドロキシステロイドデヒドロゲナーゼI型阻害剤 Download PDFInfo
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- JP5268912B2 JP5268912B2 JP2009525773A JP2009525773A JP5268912B2 JP 5268912 B2 JP5268912 B2 JP 5268912B2 JP 2009525773 A JP2009525773 A JP 2009525773A JP 2009525773 A JP2009525773 A JP 2009525773A JP 5268912 B2 JP5268912 B2 JP 5268912B2
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- 0 C(*1)OC2=C1C=CCC2 Chemical compound C(*1)OC2=C1C=CCC2 0.000 description 2
- DNNVRTZJRKIUFK-UHFFFAOYSA-N C(C1)C=Nc2c1cccc2 Chemical compound C(C1)C=Nc2c1cccc2 DNNVRTZJRKIUFK-UHFFFAOYSA-N 0.000 description 1
- BNVMAOANLNTNBL-UHFFFAOYSA-N C1C(CCCC2)=C2OC1 Chemical compound C1C(CCCC2)=C2OC1 BNVMAOANLNTNBL-UHFFFAOYSA-N 0.000 description 1
- HRCMXYXVAWHBTH-UHFFFAOYSA-N C1Oc(cccc2)c2N1 Chemical compound C1Oc(cccc2)c2N1 HRCMXYXVAWHBTH-UHFFFAOYSA-N 0.000 description 1
- YMDMRRBISDUMPR-UHFFFAOYSA-N C=CCOC1(C2C(C3)CC1CC3C2)C(CC1)=CC=C1F Chemical compound C=CCOC1(C2C(C3)CC1CC3C2)C(CC1)=CC=C1F YMDMRRBISDUMPR-UHFFFAOYSA-N 0.000 description 1
- KTRKZYFLDCADMP-UHFFFAOYSA-N CC(C)(OC(C1=C(C(CC(C2)C3)C4)C2CC34C(O)=O)=O)OC1=O Chemical compound CC(C)(OC(C1=C(C(CC(C2)C3)C4)C2CC34C(O)=O)=O)OC1=O KTRKZYFLDCADMP-UHFFFAOYSA-N 0.000 description 1
- WVDFHMDASYVAMF-UHFFFAOYSA-N COC(C(CC1(C2CC(C3)CC1CC3C2)c(cc1)ccc1F)=O)=O Chemical compound COC(C(CC1(C2CC(C3)CC1CC3C2)c(cc1)ccc1F)=O)=O WVDFHMDASYVAMF-UHFFFAOYSA-N 0.000 description 1
- NOTKBFGIXFLCEF-UHFFFAOYSA-N N#CC(C#N)=C(C(C1)CC2C3)C3C1C21OCCO1 Chemical compound N#CC(C#N)=C(C(C1)CC2C3)C3C1C21OCCO1 NOTKBFGIXFLCEF-UHFFFAOYSA-N 0.000 description 1
- AKJJLOSQVTZYQJ-UHFFFAOYSA-O N/C(/CC1(C2CC(C3)CC1CC3C2)c(cc1)ccc1F)=N\N=[NH2+] Chemical compound N/C(/CC1(C2CC(C3)CC1CC3C2)c(cc1)ccc1F)=N\N=[NH2+] AKJJLOSQVTZYQJ-UHFFFAOYSA-O 0.000 description 1
- MOXCIIZGAFOOGR-UHFFFAOYSA-N N=CCC1(C2C(C3)CC1CC3C2)c(cc1)ccc1F Chemical compound N=CCC1(C2C(C3)CC1CC3C2)c(cc1)ccc1F MOXCIIZGAFOOGR-UHFFFAOYSA-N 0.000 description 1
- GFVNJDIBQYYKGS-UHFFFAOYSA-N NC(OC1CNC1)=O Chemical compound NC(OC1CNC1)=O GFVNJDIBQYYKGS-UHFFFAOYSA-N 0.000 description 1
- ODFRBYOJLDRSKF-UHFFFAOYSA-N O=C1OC(CCCC2)=C2CC1 Chemical compound O=C1OC(CCCC2)=C2CC1 ODFRBYOJLDRSKF-UHFFFAOYSA-N 0.000 description 1
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N O=C1Oc(cccc2)c2C=C1 Chemical compound O=C1Oc(cccc2)c2C=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 1
- QWSHWQRXXGXIEL-UHFFFAOYSA-N OC(C(C1(C(C2)C34C1CC3CC2C4)c(cc1)ccc1F)C(O)=O)=O Chemical compound OC(C(C1(C(C2)C34C1CC3CC2C4)c(cc1)ccc1F)C(O)=O)=O QWSHWQRXXGXIEL-UHFFFAOYSA-N 0.000 description 1
- BFVSFISOYLHSEL-UHFFFAOYSA-N OC(C1)CN1C(CC(C(CC1)C2)(C1CC2O)c(cc1)ccc1F)=O Chemical compound OC(C1)CN1C(CC(C(CC1)C2)(C1CC2O)c(cc1)ccc1F)=O BFVSFISOYLHSEL-UHFFFAOYSA-N 0.000 description 1
- DGDNZYYLKRAEIS-UHFFFAOYSA-N OC(CC1(C2C(C3)CC1CC3C2)c(cc1)ccc1F)=O Chemical compound OC(CC1(C2C(C3)CC1CC3C2)c(cc1)ccc1F)=O DGDNZYYLKRAEIS-UHFFFAOYSA-N 0.000 description 1
- RZQBDIZIQNASEL-UHFFFAOYSA-N c(cc1)cc2c1SC=NC=C2 Chemical compound c(cc1)cc2c1SC=NC=C2 RZQBDIZIQNASEL-UHFFFAOYSA-N 0.000 description 1
- IANQTJSKSUMEQM-UHFFFAOYSA-N c1c[o]c2c1cccc2 Chemical compound c1c[o]c2c1cccc2 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 1
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| US8119658B2 (en) * | 2007-10-01 | 2012-02-21 | Bristol-Myers Squibb Company | Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors |
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| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| JP6033791B2 (ja) | 2011-12-23 | 2016-11-30 | Meiji Seikaファルマ株式会社 | 新規s1p受容体調整薬 |
| US9580422B2 (en) | 2013-10-22 | 2017-02-28 | Bristol-Myers Squibb Company | Isotopically labeled triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors |
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| NO177005C (no) | 1988-01-20 | 1995-07-05 | Bayer Ag | Analogifremgangsmåte for fremstilling av substituerte pyridiner, samt mellomprodukter til bruk ved fremstillingen |
| FI94339C (fi) | 1989-07-21 | 1995-08-25 | Warner Lambert Co | Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013173783A (ja) * | 2006-08-24 | 2013-09-05 | Bristol Myers Squibb Co | 環状11−βヒドロキシステロイドデヒドロゲナーゼI型阻害剤 |
Also Published As
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|---|---|
| AR062533A1 (es) | 2008-11-12 |
| CL2007002492A1 (es) | 2008-01-11 |
| US20080234249A1 (en) | 2008-09-25 |
| CA2661401A1 (en) | 2008-02-28 |
| MX2009001687A (es) | 2009-02-25 |
| EA200900344A1 (ru) | 2009-10-30 |
| AU2007286629A1 (en) | 2008-02-28 |
| US20100204199A1 (en) | 2010-08-12 |
| CN103833544A (zh) | 2014-06-04 |
| WO2008024892A3 (en) | 2008-12-11 |
| JP2010501589A (ja) | 2010-01-21 |
| US8299054B2 (en) | 2012-10-30 |
| JP2013173783A (ja) | 2013-09-05 |
| BRPI0715839A2 (pt) | 2013-07-23 |
| TW200817353A (en) | 2008-04-16 |
| US7727978B2 (en) | 2010-06-01 |
| WO2008024892A2 (en) | 2008-02-28 |
| EP2054368B1 (en) | 2015-09-16 |
| EP2527317A1 (en) | 2012-11-28 |
| KR20090057038A (ko) | 2009-06-03 |
| NO20090445L (no) | 2009-02-26 |
| EP2054368A2 (en) | 2009-05-06 |
| IL196989A0 (en) | 2009-11-18 |
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