Small Molecule 11β- Hydroxysteroid Dehydrogenase Type 1 Inhibitors

被引:21
|
作者
Sun, Daqing [1 ]
Wang, Minghan [2 ]
Wang, Zhulun [1 ]
机构
[1] Amgen Inc, 1120 Vet Blvd, San Francisco, CA 94080 USA
[2] Amgen Inc, Thousand Oaks, CA 91320 USA
关键词
11; beta-HSD1; beta-HSD2; metabolic syndrome; type; 2; diabetes; sulfonamide; amide; triazole; BETA-KETO SULFONES; SELECTIVE INHIBITORS; ADIPOSE-TISSUE; 11-BETA-HYDROXYSTEROID DEHYDROGENASES; GLUCOCORTICOID ACTION; METABOLIC SYNDROME; VISCERAL OBESITY; DISCOVERY; POTENT; TRIAZOLES;
D O I
10.2174/156802611795860988
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
11 beta-hydroxysteroid dehydrogenase type 1 (11 beta-HSD1) catalyzes the interconversion of inactive cortisone to active cortisol in a NADPH dependent manner. Excess cortisol or 11 beta-HSD1 leads to insulin resistance and metabolic syndrome. Inhibition of 11 beta-HSD1 activity has been pursued vigorously by the pharmaceutical industry as a potential therapeutic strategy for the treatment of type 2 diabetes. As a result, a large number of chemical classes have been identified as potent and selective small molecule inhibitors for 11 beta-HSD1. Here we review the recent progress in the discovery and development of small molecule inhibitors of 11 beta-HSD1 by highlighting the medicinal chemistry, SAR, in vivo pharmacodynamic effects and efficacy of a few representative classes of inhibitors in models of diabetes. Furthermore, we also review the structural characteristics of each class of inhibitors by analyzing the inhibitor co-crystal structures of 11 beta-HSD1.
引用
收藏
页码:1464 / 1475
页数:12
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