化学
差向异构体
立体化学
异丙基
体内
双环分子
体外
酶抑制剂
非对映体
脱氢酶
酶
药理学
生物化学
药物化学
生物技术
生物
医学
作者
Murielle M. Véniant,Clarence Hale,Randall W. Hungate,Kyung H. Gahm,Maurice G. Emery,Janan Jona,Smriti Joseph,Jeffrey A. Adams,Andrew B. Hague,George A. Moniz,Jiandong Zhang,Michael D. Bartberger,Vivian Li,Rashid Syed,Steven R. Jordan,Renée Komorowski,Michelle Chen,Rod Cupples,Ki Won Kim,David J. St. Jean
摘要
Thiazolones with an exo-norbornylamine at the 2-position and an isopropyl group on the 5-position are potent 11beta-HSD1 inhibitors. However, the C-5 center was prone to epimerization in vitro and in vivo, forming a less potent diastereomer. A methyl group was added to the C-5 position to eliminate epimerization, leading to the discovery of (S)-2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one (AMG 221). This compound decreased fed blood glucose and insulin levels and reduced body weight in diet-induced obesity mice.
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