药理学
生物利用度
敌手
CCR2型
药代动力学
微粒体
趋化因子受体
CCR5受体拮抗剂
化学
医学
趋化因子
受体
生物化学
体外
作者
Robert J. Cherney,Prakash Anjanappa,K. Selvakumar,Douglas G. Batt,Gregory D. Brown,Anne Rose,Ragini Vuppugalla,Jing Chen,Jian Pang,Songmei Xu,Melissa Yarde,Andrew J. Tebben,Venkatram Reddy Paidi,Mary Ellen Cvijic,Arvind Mathur,Joel C. Barrish,Sandhya Mandlekar,Qihong Zhao,Percy H. Carter
标识
DOI:10.1021/acsmedchemlett.1c00373
摘要
BMS-813160 (compound 3) was identified as a potent and selective CCR2/5 dual antagonist. Compound 3 displayed good permeability at pH = 7.4 in PAMPA experiments and demonstrated excellent human liver microsome stability. Pharmacokinetic studies established that 3 had excellent oral bioavailability and exhibited low clearance in dog and cyno. Compound 3 was also studied in the mouse thioglycollate-induced peritonitis model, which confirmed its ability to inhibit the migration of inflammatory monocytes and macrophages. As a result of this profile, compound 3 was selected as a clinical candidate.
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