吲哚
化学
赫拉
效力
立体化学
体外
结构-活动关系
药理学
组合化学
生物化学
医学
作者
Wensheng Yu,Yongqi Deng,Brett A. Hopkins,Xianhai Huang,David L. Sloman,Hongjun Zhang,Derun Li,Meredeth A. McGowan,Catherine A. White,Qinglin Pu,K. Liu,Xavier Fradera,Charles A. Lesburg,Theodore A. Martinot,Amy C. Doty,Heidi M. Ferguson,Elliott Nickbarg,Mangeng Cheng,Prasanthi Geda,Xuelei S. Song
标识
DOI:10.1016/j.bmcl.2021.128214
摘要
A novel series of IDO1 inhibitors have been identified with good IDO1 Hela cell and human whole blood activity. These inhibitors contain an indoline or a 3-azaindoline scaffold. Their structure-activity-relationship studies have been explored. Compounds 37 and 41 stood out as leads due to their good potency in IDO1 Hela assay, good IDO1 unbound hWB IC50s, reasonable unbound clearance, and good MRT in rat and dog PK studies.
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