| Literature DB >> 25313327 |
Prabhakar K Jadhav1, Matthew A Schiffler1, Kostas Gavardinas1, Euibong J Kim1, Donald P Matthews1, Michael A Staszak1, D Scott Coffey1, Bruce W Shaw1, Kenneth C Cassidy1, Richard A Brier1, Yuke Zhang1, Robert M Christie1, William F Matter1, Keyun Qing1, Jim D Durbin1, Yong Wang1, Gary G Deng1.
Abstract
Cathepsin S (Cat S) plays an important role in many pathological conditions, including abdominal aortic aneurysm (AAA). Inhibition of Cat S may provide a new treatment for AAA. To date, several classes of Cat S inhibitors have been reported, many of which form covalent interactions with the active site Cys25. Herein, we report the discovery of a novel series of noncovalent inhibitors of Cat S through a medium-throughput focused cassette screen and the optimization of the resulting hits. Structure-based optimization efforts led to Cat S inhibitors such as 5 and 9 with greatly improved potency and drug disposition properties. This series of compounds binds to the S2 and S3 subsites without interacting with the active site Cys25. On the basis of in vitro potency, selectivity, and efficacy in a CaCl2-induced AAA in vivo model, 5 (LY3000328) was selected for clinical development.Entities:
Keywords: Cathepsin; abdominal aortic aneurysm; development candidate; noncovalent
Year: 2014 PMID: 25313327 PMCID: PMC4190634 DOI: 10.1021/ml500283g
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345