Discovery and optimization of piperidyl benzamide derivatives as a novel class of 11β-HSD1 inhibitors

The discovery and optimization of a piperidyl benzamide series of 11β-HSD1 inhibitors is reported. Discovery and optimization of a piperidyl benzamide series of 11β-HSD1 inhibitors is described. This series was derived from a cyclohexyl benzamide lead structures to address PXR selectivity, high non-...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2009-03, Vol.19 (6), p.1797-1801
Hauptverfasser: Rew, Yosup, McMinn, Dustin L., Wang, Zhulun, He, Xiao, Hungate, Randall W., Jaen, Juan C., Sudom, Athena, Sun, Daqing, Tu, Hua, Ursu, Stefania, Villemure, Elisia, Walker, Nigel P.C., Yan, Xuelei, Ye, Qiuping, Powers, Jay P.
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Sprache:eng
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Zusammenfassung:The discovery and optimization of a piperidyl benzamide series of 11β-HSD1 inhibitors is reported. Discovery and optimization of a piperidyl benzamide series of 11β-HSD1 inhibitors is described. This series was derived from a cyclohexyl benzamide lead structures to address PXR selectivity, high non-specific protein binding, poor solubility, limited in vivo exposure, and in vitro cytotoxicity issues observed with the cyclohexyl benzamide structures. These efforts led to the discovery of piperidyl benzamide 15 which features improved properties over the cyclohexyl benzamide derivatives.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2009.01.058