期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 18, 期 3, 页码 942-945出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2007.12.038
关键词
NHERF1; EBP50; PDZ domain; protein-protein interaction inhibitor; indole; small molecule
This report describes the first small-molecule antagonists that specifically target the ligand-binding pocket of PDZ domains of NHERF1 multi-functional adaptor protein. Comparison of the peptide sequence homology between the native ligand of NHERF1 PDZ domains and an indole-based non-peptide chemical scaffold allowed the design of a small-molecule antagonist of NHERF1 PDZ domains. (C) 2007 Elsevier Ltd. All rights reserved.
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