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Design and synthesis of 3,7-diarylimidazopyridines as inhibitors of the VEGF-receptor KDR
Authors:Wu Zhicai  Fraley Mark E  Bilodeau Mark T  Kaufman Mildred L  Tasber Edward S  Balitza Adrienne E  Hartman George D  Coll Kathleen E  Rickert Keith  Shipman Jennifer  Shi Bin  Sepp-Lorenzino Laura  Thomas Kenneth A
Affiliation:Department of Medicinal Chemistry, Merck Research Laboratories, PO Box 4, West Point, PA 19486, USA. zhicai_wu@merck.com
Abstract:3,7-Diarylsubstituted imidazopyridines were designed and developed as a new class of KDR kinase inhibitors. A variety of imidazopyridines were synthesized and potent inhibitors of KDR kinase activity were identified with good aqueous solubility.
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