Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1367156 | Bioorganic & Medicinal Chemistry Letters | 2006 | 5 Pages |
Abstract
A series of potent and selective adamantane aminoamide 11-β-HSD-1 inhibitors has been optimized. Chemically these studies were expedited by utilizing readily obtained amino acids as starting materials or an isocyanide multicomponent reaction. Structure–activity relationship studies resulted in the discovery of dual human and mouse 11-β-HSD-1 potent and selective inhibitors like adamantane 11 and related compounds with high metabolic stability and robust pharmacokinetic profiles.
Graphical abstractThe synthesis of the potent and selective h-11-β-HSD-1 inhibitor 11 (Ki = 8 nm) is reported.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Bryan Sorensen, Jeff Rohde, Jiahong Wang, Steven Fung, Katina Monzon, William Chiou, Liping Pan, Xiaoqing Deng, DeAnne Stolarik, Ernst U. Frevert, Peer Jacobson, J.T. Link,