2. Academic Validation
  3. Discovery of INCB3344, a potent, selective and orally bioavailable antagonist of human and murine CCR2

Discovery of INCB3344, a potent, selective and orally bioavailable antagonist of human and murine CCR2

  • Bioorg Med Chem Lett. 2010 Dec 15;20(24):7473-8. doi: 10.1016/j.bmcl.2010.10.020.
Chu-Biao Xue 1,  Anlai Wang,  David Meloni,  Ke Zhang,  Ling Kong,  Hao Feng,  Joseph Glenn,  Taisheng Huang,  Yingxin Zhang,  Ganfeng Cao,  Rajan Anand,  Changsheng Zheng,  Michael Xia,  Qi Han,  D J Robinson,  Lou Storace,  Lixin Shao,  Mei Li,  Carrie M Brodmerkel,  Maryanne Covington,  Peggy Scherle,  Sharon Diamond,  Swamy Yeleswaram,  Kris Vaddi,  Robert Newton,  Greg Hollis,  Steven Friedman,  Brian Metcalf
Affiliations

Affiliation

  • 1 Incyte Corporation, Experimental Station E336, Wilmington, DE 19880, USA. cxue@incyte.com
PMID: 21036044 DOI: 10.1016/j.bmcl.2010.10.020
Abstract

Rational design based on a pharmacophore of CCR2 antagonists reported in the literature identified lead compound 9a with potent inhibitory activity against human CCR2 (hCCR2) but moderate activity against murine CCR2 (mCCR2). Modification on 9a led to the discovery of a potent CCR2 Antagonist 21 (INCB3344) with IC(50) values of 5.1 nM (hCCR2) and 9.5 nM (mCCR2) in binding antagonism and 3.8 nM (hCCR2) and 7.8 nM (mCCR2) in antagonism of chemotaxis activity. INCB3344 exhibited >100-fold selectivity over Other homologous chemokine receptors, a free fraction of 24% in human serum and 15% in mouse serum, and an oral bioavailability of 47% in mice, suitable as a tool compound for target validation in rodent models.

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