JP2009535362A5 - - Google Patents
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- Publication number
- JP2009535362A5 JP2009535362A5 JP2009507978A JP2009507978A JP2009535362A5 JP 2009535362 A5 JP2009535362 A5 JP 2009535362A5 JP 2009507978 A JP2009507978 A JP 2009507978A JP 2009507978 A JP2009507978 A JP 2009507978A JP 2009535362 A5 JP2009535362 A5 JP 2009535362A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- pyrrolidin
- ylmethyl
- dichloro
- biphenyl
- 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.)
- Granted
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- 229910052736 halogen Inorganic materials 0.000 claims 25
- 150000002367 halogens Chemical class 0.000 claims 25
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 16
- 239000001257 hydrogen Substances 0.000 claims 16
- 229910052739 hydrogen Inorganic materials 0.000 claims 16
- 150000003839 salts Chemical class 0.000 claims 10
- 239000011780 sodium chloride Substances 0.000 claims 10
- 150000001875 compounds Chemical class 0.000 claims 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 9
- 150000002431 hydrogen Chemical class 0.000 claims 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 4
- 125000004093 cyano group Chemical group *C#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
- GKBQUUWPGKYVCC-INIZCTEOSA-N 4-[(3R)-3-[[2,6-dichloro-4-(4-fluorophenyl)phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1N1C(=O)[C@H](CC=2C(=CC(=CC=2Cl)C=2C=CC(F)=CC=2)Cl)CC1 GKBQUUWPGKYVCC-INIZCTEOSA-N 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- ZOJLBBQEBUMFCU-INIZCTEOSA-N (3R)-3-[[2,6-dichloro-4-(4-fluorophenyl)phenyl]methyl]-1-(1-methylsulfonylpiperidin-4-yl)pyrrolidin-2-one Chemical compound C1CN(S(=O)(=O)C)CCC1N1C(=O)[C@H](CC=2C(=CC(=CC=2Cl)C=2C=CC(F)=CC=2)Cl)CC1 ZOJLBBQEBUMFCU-INIZCTEOSA-N 0.000 claims 1
- CNNLTMSBPIKXPM-UHFFFAOYSA-N 3-[[2,6-dichloro-4-[4-[4-(2,2,2-trifluoroethyl)piperazine-1-carbonyl]phenyl]phenyl]methyl]-1-(1-methylsulfonylpiperidin-4-yl)pyrrolidin-2-one Chemical compound C1CN(S(=O)(=O)C)CCC1N1C(=O)C(CC=2C(=CC(=CC=2Cl)C=2C=CC(=CC=2)C(=O)N2CCN(CC(F)(F)F)CC2)Cl)CC1 CNNLTMSBPIKXPM-UHFFFAOYSA-N 0.000 claims 1
- WDQVDGUKAPWZNZ-SFHVURJKSA-N 4-[(3R)-3-[[2,6-dichloro-4-(4-cyanophenyl)phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1N1C(=O)[C@H](CC=2C(=CC(=CC=2Cl)C=2C=CC(=CC=2)C#N)Cl)CC1 WDQVDGUKAPWZNZ-SFHVURJKSA-N 0.000 claims 1
- ILFLDZSMSGFGTJ-FQEVSTJZSA-N 4-[(3R)-3-[[2,6-dichloro-4-(4-fluorophenyl)phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-phenylpiperidine-1-carboxamide Chemical compound C1=CC(F)=CC=C1C(C=C1Cl)=CC(Cl)=C1C[C@H]1C(=O)N(C2CCN(CC2)C(=O)NC=2C=CC=CC=2)CC1 ILFLDZSMSGFGTJ-FQEVSTJZSA-N 0.000 claims 1
- FXCOPNPNUHWSTQ-IBGZPJMESA-N 4-[(3R)-3-[[2,6-dichloro-4-(4-propan-2-yloxyphenyl)phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1N1C(=O)[C@H](CC=2C(=CC(=CC=2Cl)C=2C=CC(OC(C)C)=CC=2)Cl)CC1 FXCOPNPNUHWSTQ-IBGZPJMESA-N 0.000 claims 1
- KZOLFEWPGNJGIJ-INIZCTEOSA-N 4-[(3R)-3-[[2,6-dichloro-4-[4-(trifluoromethoxy)phenyl]phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1N1C(=O)[C@H](CC=2C(=CC(=CC=2Cl)C=2C=CC(OC(F)(F)F)=CC=2)Cl)CC1 KZOLFEWPGNJGIJ-INIZCTEOSA-N 0.000 claims 1
- WDRZOMROYRDRKS-INIZCTEOSA-N 4-[(3R)-3-[[2,6-dichloro-4-[4-(trifluoromethyl)phenyl]phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1N1C(=O)[C@H](CC=2C(=CC(=CC=2Cl)C=2C=CC(=CC=2)C(F)(F)F)Cl)CC1 WDRZOMROYRDRKS-INIZCTEOSA-N 0.000 claims 1
- XXOCJEDPQIFLAQ-NRFANRHFSA-N 4-[(3R)-3-[[2,6-dichloro-4-[4-[4-(trifluoromethyl)piperidine-1-carbonyl]phenyl]phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1N1C(=O)[C@H](CC=2C(=CC(=CC=2Cl)C=2C=CC(=CC=2)C(=O)N2CCC(CC2)C(F)(F)F)Cl)CC1 XXOCJEDPQIFLAQ-NRFANRHFSA-N 0.000 claims 1
- VFZYXSQMAWPNHV-UHFFFAOYSA-N 4-[3-[[2,6-dichloro-4-(4-fluorophenyl)phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-ethylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NCC)CCC1N1C(=O)C(CC=2C(=CC(=CC=2Cl)C=2C=CC(F)=CC=2)Cl)CC1 VFZYXSQMAWPNHV-UHFFFAOYSA-N 0.000 claims 1
- KXHWIUXOFOFHOF-UHFFFAOYSA-N 4-[3-[[2,6-dichloro-4-(4-fluorophenyl)phenyl]methyl]-2-oxopyrrolidin-1-yl]piperidine-1-carboxamide Chemical compound C1CN(C(=O)N)CCC1N1C(=O)C(CC=2C(=CC(=CC=2Cl)C=2C=CC(F)=CC=2)Cl)CC1 KXHWIUXOFOFHOF-UHFFFAOYSA-N 0.000 claims 1
- BPGFEKRMECDIQC-UHFFFAOYSA-N 4-[3-[[2,6-dichloro-4-(4-methylphenyl)phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1N1C(=O)C(CC=2C(=CC(=CC=2Cl)C=2C=CC(C)=CC=2)Cl)CC1 BPGFEKRMECDIQC-UHFFFAOYSA-N 0.000 claims 1
- FXCOPNPNUHWSTQ-UHFFFAOYSA-N 4-[3-[[2,6-dichloro-4-(4-propan-2-yloxyphenyl)phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1N1C(=O)C(CC=2C(=CC(=CC=2Cl)C=2C=CC(OC(C)C)=CC=2)Cl)CC1 FXCOPNPNUHWSTQ-UHFFFAOYSA-N 0.000 claims 1
- JQRXICJLNSCYTB-UHFFFAOYSA-N 4-[3-[[2,6-dichloro-4-[2-(trifluoromethyl)phenyl]phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1N1C(=O)C(CC=2C(=CC(=CC=2Cl)C=2C(=CC=CC=2)C(F)(F)F)Cl)CC1 JQRXICJLNSCYTB-UHFFFAOYSA-N 0.000 claims 1
- PYVLUSPYWYDNQG-UHFFFAOYSA-N 4-[3-[[2,6-dichloro-4-[3-(trifluoromethyl)phenyl]phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1N1C(=O)C(CC=2C(=CC(=CC=2Cl)C=2C=C(C=CC=2)C(F)(F)F)Cl)CC1 PYVLUSPYWYDNQG-UHFFFAOYSA-N 0.000 claims 1
- WDRZOMROYRDRKS-UHFFFAOYSA-N 4-[3-[[2,6-dichloro-4-[4-(trifluoromethyl)phenyl]phenyl]methyl]-2-oxopyrrolidin-1-yl]-N-methylpiperidine-1-carboxamide Chemical compound C1CN(C(=O)NC)CCC1N1C(=O)C(CC=2C(=CC(=CC=2Cl)C=2C=CC(=CC=2)C(F)(F)F)Cl)CC1 WDRZOMROYRDRKS-UHFFFAOYSA-N 0.000 claims 1
- NPXWHTKMKGVLEG-FQEVSTJZSA-N N-cyclohexyl-4-[(3R)-3-[[2,6-dichloro-4-(4-fluorophenyl)phenyl]methyl]-2-oxopyrrolidin-1-yl]piperidine-1-carboxamide Chemical compound C1=CC(F)=CC=C1C(C=C1Cl)=CC(Cl)=C1C[C@H]1C(=O)N(C2CCN(CC2)C(=O)NC2CCCCC2)CC1 NPXWHTKMKGVLEG-FQEVSTJZSA-N 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- RNABFKLYNRWJML-INIZCTEOSA-N methyl 4-[(3R)-3-[[2,6-dichloro-4-(4-fluorophenyl)phenyl]methyl]-2-oxopyrrolidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C(=O)[C@H](CC=2C(=CC(=CC=2Cl)C=2C=CC(F)=CC=2)Cl)CC1 RNABFKLYNRWJML-INIZCTEOSA-N 0.000 claims 1
- KMLQOMUMWAYYCW-NRFANRHFSA-N methyl 4-[(3R)-3-[[2,6-dichloro-4-[4-[4-(trifluoromethyl)piperidine-1-carbonyl]phenyl]phenyl]methyl]-2-oxopyrrolidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C(=O)[C@H](CC=2C(=CC(=CC=2Cl)C=2C=CC(=CC=2)C(=O)N2CCC(CC2)C(F)(F)F)Cl)CC1 KMLQOMUMWAYYCW-NRFANRHFSA-N 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- HZZCSLKKNXVQSN-UHFFFAOYSA-N CC(N(CC1)CCC1(F)F)=O Chemical compound CC(N(CC1)CCC1(F)F)=O HZZCSLKKNXVQSN-UHFFFAOYSA-N 0.000 description 1
- 0 CC(N1CC(O*)OC(*)C1)=O Chemical compound CC(N1CC(O*)OC(*)C1)=O 0.000 description 1
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US79611206P | 2006-04-28 | 2006-04-28 | |
US60/796,112 | 2006-04-28 | ||
PCT/US2007/067597 WO2007127901A1 (en) | 2006-04-28 | 2007-04-27 | Pieridinyl substituted pyrrolidinones as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2009535362A JP2009535362A (ja) | 2009-10-01 |
JP2009535362A5 true JP2009535362A5 (US07981874-20110719-C00313.png) | 2010-05-13 |
JP5225980B2 JP5225980B2 (ja) | 2013-07-03 |
Family
ID=38421166
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2009507978A Expired - Fee Related JP5225980B2 (ja) | 2006-04-28 | 2007-04-27 | 11−β−ヒドロキシステロイドデヒドロゲナーゼ1の阻害剤としてのピエリジニル置換ピロリジノン |
Country Status (23)
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2029576B1 (en) | 2006-04-21 | 2013-06-19 | Eli Lilly & Company | Cyclohexylimidazole lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
US7981918B2 (en) | 2006-04-21 | 2011-07-19 | Eli Lilly And Company | Cyclohexylpyrazole-lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
EA014718B1 (ru) * | 2006-04-21 | 2011-02-28 | Эли Лилли Энд Компани | Производные бифениламидлактама в качестве ингибиторов 11-бета-гидроксистероиддегидрогеназы 1 |
WO2007127693A1 (en) | 2006-04-24 | 2007-11-08 | Eli Lilly And Company | Substituted pyrrolidinones as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
JP5118692B2 (ja) | 2006-04-24 | 2013-01-16 | イーライ リリー アンド カンパニー | 11−β−ヒドロキシステロイドデヒドロゲナーゼ1の阻害剤としてのシクロヘキシル置換ピロリジノン |
EP2021336B1 (en) | 2006-04-24 | 2010-06-30 | Eli Lilly And Company | Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
MX2008013656A (es) | 2006-04-25 | 2008-11-10 | Lilly Co Eli | Inhibidores de 11-beta-hidroxiesteroide deshidrogenasa. |
DK2021337T3 (da) | 2006-04-25 | 2010-03-29 | Lilly Co Eli | Inhibitorer af 11-beta-hydroxysteroid-dehydrogenase-1 |
WO2007127763A2 (en) | 2006-04-25 | 2007-11-08 | Eli Lilly And Company | Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
EP2243479A3 (en) | 2009-04-20 | 2011-01-19 | Abbott Laboratories | Novel amide and amidine derivates and uses thereof |
US8871208B2 (en) * | 2009-12-04 | 2014-10-28 | Abbvie Inc. | 11-β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitors and uses thereof |
WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
EP2683700B1 (de) | 2011-03-08 | 2015-02-18 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
WO2012120055A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
US8828994B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
US8828995B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
US8901114B2 (en) | 2011-03-08 | 2014-12-02 | Sanofi | Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof |
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 |
KR101593493B1 (ko) | 2014-10-28 | 2016-02-18 | 주식회사 아이에스티이 | 대면적 유리기판 열처리 장치 |
Family Cites Families (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR0315166A (pt) * | 2002-10-11 | 2005-08-16 | Astrazeneca Ab | Uso de um composto ou de um sal farmaceuticamente aceitável do mesmo, composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, e, método para produzir um efeito inibidor de 11betahsd1 em um animal de sangue quente, tal como o homem, que necessita de tratamento |
WO2004056744A1 (en) | 2002-12-23 | 2004-07-08 | Janssen Pharmaceutica N.V. | Adamantyl acetamides as hydroxysteroid dehydrogenase inhibitors |
JP5014983B2 (ja) * | 2004-05-07 | 2012-08-29 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 11−ベータヒドロキシステロイドデヒドロゲナーゼ阻害剤としてのピロリジン−2−オン及びピペリジン−2−オン誘導体 |
WO2005108361A1 (en) * | 2004-05-07 | 2005-11-17 | Janssen Pharmaceutica N.V. | Adamantyl pyrrolidin-2-one derivatives as 11-beta hydroxysteroid dehydrogenase inhibitors |
US8138342B2 (en) | 2004-10-12 | 2012-03-20 | High Point Pharmacueticals, LLC | 11β-hydroxysteroid dehydrogenase type 1 active spiro compounds |
ATE419848T1 (de) | 2004-10-29 | 2009-01-15 | Lilly Co Eli | Cycloalkyl-lactam-derivate als inhibitoren von 11-beta-hydroxysteroiddehydrogenase 1 |
EA019747B1 (ru) | 2004-11-10 | 2014-06-30 | Инсайт Корпорейшн | Лактамные соединения и их применение в качестве фармацевтических препаратов |
ES2308602T3 (es) | 2004-12-20 | 2008-12-01 | Eli Lilly And Company | Derivados de cicloalquil lactamas como inhibidores de la 11-beta-hidroxiesteroide deshidrogenasa 1. |
WO2006068991A1 (en) | 2004-12-21 | 2006-06-29 | Eli Lilly And Company | Cycloalkyl lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
EP1864971A4 (en) | 2005-03-31 | 2010-02-10 | Takeda Pharmaceutical | PROPHYLACTIC / THERAPEUTIC AGENT AGAINST DIABETES |
WO2007084314A2 (en) | 2006-01-12 | 2007-07-26 | Incyte Corporation | MODULATORS OF 11-ß HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME |
EA014718B1 (ru) | 2006-04-21 | 2011-02-28 | Эли Лилли Энд Компани | Производные бифениламидлактама в качестве ингибиторов 11-бета-гидроксистероиддегидрогеназы 1 |
EP2029576B1 (en) | 2006-04-21 | 2013-06-19 | Eli Lilly & Company | Cyclohexylimidazole lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
US7981918B2 (en) | 2006-04-21 | 2011-07-19 | Eli Lilly And Company | Cyclohexylpyrazole-lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
JP5118692B2 (ja) | 2006-04-24 | 2013-01-16 | イーライ リリー アンド カンパニー | 11−β−ヒドロキシステロイドデヒドロゲナーゼ1の阻害剤としてのシクロヘキシル置換ピロリジノン |
WO2007127693A1 (en) | 2006-04-24 | 2007-11-08 | Eli Lilly And Company | Substituted pyrrolidinones as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
EP2021336B1 (en) | 2006-04-24 | 2010-06-30 | Eli Lilly And Company | Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
DK2021337T3 (da) | 2006-04-25 | 2010-03-29 | Lilly Co Eli | Inhibitorer af 11-beta-hydroxysteroid-dehydrogenase-1 |
WO2007127763A2 (en) | 2006-04-25 | 2007-11-08 | Eli Lilly And Company | Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
MX2008013656A (es) | 2006-04-25 | 2008-11-10 | Lilly Co Eli | Inhibidores de 11-beta-hidroxiesteroide deshidrogenasa. |
CL2008001839A1 (es) | 2007-06-21 | 2009-01-16 | Incyte Holdings Corp | Compuestos derivados de 2,7-diazaespirociclos, inhibidores de 11-beta hidroxil esteroide deshidrogenasa tipo 1; composicion farmaceutica que comprende a dichos compuestos; utiles para tratar la obesidad, diabetes, intolerancia a la glucosa, diabetes tipo ii, entre otras enfermedades. |
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2007
- 2007-04-27 KR KR1020087026195A patent/KR101060016B1/ko not_active IP Right Cessation
- 2007-04-27 MX MX2008013844A patent/MX2008013844A/es active IP Right Grant
- 2007-04-27 AT AT07761424T patent/ATE542811T1/de active
- 2007-04-27 US US12/297,951 patent/US7829582B2/en not_active Expired - Fee Related
- 2007-04-27 DK DK07761424.6T patent/DK2049513T3/da active
- 2007-04-27 EA EA200870489A patent/EA014719B1/ru not_active IP Right Cessation
- 2007-04-27 PL PL07761424T patent/PL2049513T3/pl unknown
- 2007-04-27 EP EP07761424A patent/EP2049513B1/en active Active
- 2007-04-27 BR BRPI0710469-3A patent/BRPI0710469A2/pt not_active IP Right Cessation
- 2007-04-27 PT PT07761424T patent/PT2049513E/pt unknown
- 2007-04-27 SI SI200730872T patent/SI2049513T1/sl unknown
- 2007-04-27 CN CN2007800154205A patent/CN101448816B/zh not_active Expired - Fee Related
- 2007-04-27 WO PCT/US2007/067597 patent/WO2007127901A1/en active Application Filing
- 2007-04-27 CA CA2650627A patent/CA2650627C/en not_active Expired - Fee Related
- 2007-04-27 AU AU2007244742A patent/AU2007244742B2/en not_active Ceased
- 2007-04-27 JP JP2009507978A patent/JP5225980B2/ja not_active Expired - Fee Related
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2008
- 2008-10-15 ZA ZA200808816A patent/ZA200808816B/xx unknown
- 2008-10-23 IL IL194879A patent/IL194879A0/en unknown
- 2008-10-24 TN TNP2008000432A patent/TNSN08432A1/en unknown
- 2008-10-27 EC EC2008008849A patent/ECSP088849A/es unknown
- 2008-11-19 NO NO20084874A patent/NO20084874L/no not_active Application Discontinuation
- 2008-11-20 MA MA31397A patent/MA30421B1/fr unknown
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2012
- 2012-03-08 CY CY20121100235T patent/CY1112466T1/el unknown