Synthesis and optimization of novel 4,4-disubstituted cyclohexylbenzamide derivatives as potent 11β-HSD1 inhibitors
摘要:
The synthesis and SAR of a series of 4,4-disubstituted cyclohexylbenzamide inhibitors of 11 beta-HSD1 are described. Optimization rapidly led to potent, highly selective, and orally bioavailable inhibitors demonstrating efficacy in both rat and non-human primate ex vivo pharmacodynamic models. (c) 2010 Elsevier Ltd. All rights reserved.
Benzamide derivatives of formula I are described and have therapeutic utility, particularly in the treatment of diabetes, obesity and related conditions and disorders:
wherein R
1
, R
2
, R
3
, R
4
, R
5
, R
6
, R
7
, R
8
, and n are as defined herein.
BENZAMIDE DERIVATIVES AS MODULATORS OF 11BETA-HSD1 FOR TREATING DIABETES AND OBESITY
申请人:Amgen Inc.
公开号:EP2044004B1
公开(公告)日:2012-08-15
US8772296B2
申请人:——
公开号:US8772296B2
公开(公告)日:2014-07-08
[EN] BENZAMIDE DERIVATIVES AND USES RELATED THERETO<br/>[FR] DÉRIVÉS DE BENZAMIDE ET UTILISATIONS ASSOCIÉES À CEUX-CI
申请人:AMGEN INC
公开号:WO2007145835A2
公开(公告)日:2007-12-21
[EN] Benzamide derivatives of formula ( I ) are described and have therapeutic utility, particularly in the treatment of diabetes, obesity and related conditions and disorders, formula (I), wherein R1, R 2, R 3, R 4, R 5, R 6, R 7, R 8, and n are as defined herein. [FR] La présente invention concerne des dérivés de benzamide de formule (I) ayant une utilité thérapeutique, en particulier dans le traitement du diabète, de l'obésité et de pathologies et troubles apparentés, formule (I), où R1, R2, R3, R4, R5, R6, R7, R8, et n sont comme présentement défini.
Synthesis and optimization of novel 4,4-disubstituted cyclohexylbenzamide derivatives as potent 11β-HSD1 inhibitors
作者:Daqing Sun、Zhulun Wang、Seb Caille、Michael DeGraffenreid、Felix Gonzalez-Lopez de Turiso、Randall Hungate、Juan C. Jaen、Ben Jiang、Lisa D. Julian、Ron Kelly、Dustin L. McMinn、Jacob Kaizerman、Yosup Rew、Athena Sudom、Hua Tu、Stefania Ursu、Nigel Walker、Maren Willcockson、Xuelei Yan、Qiuping Ye、Jay P. Powers
DOI:10.1016/j.bmcl.2010.10.129
日期:2011.1
The synthesis and SAR of a series of 4,4-disubstituted cyclohexylbenzamide inhibitors of 11 beta-HSD1 are described. Optimization rapidly led to potent, highly selective, and orally bioavailable inhibitors demonstrating efficacy in both rat and non-human primate ex vivo pharmacodynamic models. (c) 2010 Elsevier Ltd. All rights reserved.