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Discovery of INCB9471, a Potent, Selective, and Orally Bioavailable CCR5 Antagonist with Potent Anti-HIV-1 Activity

  作者 XUE CHUBIAO; CHEN LIHUA; CAO GANFENG; ZHANG KE; WANG ANLAI; MELONI DAVID; GLENN JOSEPH; ANAND RAJAN; XIA MICHAEL; KONG LING; HUANG TAISHENG; FENG HAO; ZHENG CHANGSHENG; LI MEI; GALYA LAURINE; ZHOU JIACHENG; SHIN NIU; BARIBAUD FREDRIC; SOLOMON KIM; SCHERLE PEGGY; ZHAO BITAO; DIAMOND SHARON; EMM TOM; KELLER DOUGLAS; CONTEL NANCY; YELESWARAM SWAMY; VADDI KRIS; HOLLIS GREGORY; NEWTON ROBERT; FRIEDMAN STEVEN; METCALF BRIAN  
  选自 期刊  ACS Medicinal Chemistry Letters;  卷期  2010年1-9;  页码  483-487  
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[摘要]To identify a CCR5 antagonist as an HIV-1 entry inhibitor, we designed a novel series of indane derivatives based on conformational considerations. Modification on the indane ring led to the discovery of compound 22a (INCB9471) that exhibited high affinity for CCR5, potent anti-HIV-1 activity, high receptor selectivity, excellent oral bioavailability, and a tolerated safety profile. INCB9471 has entered human clinical trials.

 
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