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Design and Synthesis of 3,7-diarylimidazopyridines As Inhibitors of the VEGF-receptor KDR

Overview
Specialty Biochemistry
Date 2004 Mar 12
PMID 15012992
Citations 9
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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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