期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 20, 期 4, 页码 1405-1409出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2009.12.109
关键词
6-Benzyloxyquinolines; c-Met; Kinase inhibitor
A novel quinoline derivative that selectively inhibits c-Met kinase was identified. The molecular design is based on a result of the analysis of a PF-2341066 (1)/c-Met cocrystal structure (PDB code: 2wgj). The kinase selectivity of the derivatives is discussed from the view point of the sequence homology of the kinases, the key interactions found in X-ray cocrystal structures, and the structure-activity relationship (SAR) obtained in this work. (C) 2010 Elsevier Ltd. All rights reserved.
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