Lin Linus S, Lanza Thomas J, Jewell James P, Liu Ping, Shah Shrenik K, Qi Hongbo, Tong Xinchun, Wang Junying, Xu Suoyu S, Fong Tung M, Shen Chun-Pyn, Lao Julie, Xiao Jing Chen, Shearman Lauren P, Stribling D Sloan, Rosko Kimberly, Strack Alison, Marsh Donald J, Feng Yue, Kumar Sanjeev, Samuel Koppara, Yin Wenji, Van der Ploeg Lex H T, Goulet Mark T, Hagmann William K
Department of Medicinal Chemistry, Merck Research Laboratories, Rahway, NJ 07065, USA.
J Med Chem. 2006 Dec 28;49(26):7584-7. doi: 10.1021/jm060996+.
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.
描述了新型无环酰胺大麻素-1受体反向激动剂的发现。它们具有强效、选择性、口服生物利用度高的特点,并且在食物摄入和体重减轻的啮齿动物模型中具有活性。优化过程的一个主要重点是提高体内疗效并降低形成反应性代谢物的可能性。这些努力导致鉴定出化合物48作为治疗肥胖症的临床候选药物进行开发。