| Literature DB >> 17181138 |
Linus S Lin1, Thomas J Lanza, James P Jewell, Ping Liu, Shrenik K Shah, Hongbo Qi, Xinchun Tong, Junying Wang, Suoyu S Xu, Tung M Fong, Chun-Pyn Shen, Julie Lao, Jing Chen Xiao, Lauren P Shearman, D Sloan Stribling, Kimberly Rosko, Alison Strack, Donald J Marsh, Yue Feng, Sanjeev Kumar, Koppara Samuel, Wenji Yin, Lex H T Van der Ploeg, Mark T Goulet, William K Hagmann.
Abstract
The discovery of novel acyclic amide cannabinoid-1 receptor inverse agonists is described. They are potent, selective, orally bioavailable, and active in rodent models of food intake and body weight reduction. A major focus of the optimization process was to increase in vivo efficacy and to reduce the potential for formation of reactive metabolites. These efforts led to the identification of compound 48 for development as a clinical candidate for the treatment of obesity.Entities:
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Year: 2006 PMID: 17181138 DOI: 10.1021/jm060996+
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446