| Literature DB >> 20371178 |
Cheng Guo1, Peter R Guzzo, Mark Hadden, Bruce J Sargent, Larry Yet, Yanqing Kan, Oksana Palyha, Theresa M Kelly, Xiaoming Guan, Kim Rosko, Karen Gagen, Joseph M Metzger, Jasminka Dragovic, Kathryn Lyons, Linus S Lin, Ravi P Nargund.
Abstract
The original structure of a high-throughput screening hit obtained from an external vendor was revised based on multiple NMR studies. The active compound was re-synthesized via a novel route and its structure and biological activity as a BRS-3 agonist were unambiguously confirmed. Multi-gram quantities of the hit were prepared for pharmacokinetic and efficacy studies. The synthetic strategy allowed for the preparation of multiple analogs for SAR exploration. 2010 Elsevier Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 20371178 DOI: 10.1016/j.bmcl.2010.03.065
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823