期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 13, 期 3, 页码 499-502出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0960-894X(02)00991-5
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The design, synthesis, and biological evaluation of 1,4-diazepane-2-ones as novel LFA-1 antagonists from a scaffold-based combinatorial library are described. Initial optimization of the library lead has resulted in high-affinity antagonists of the LFA-1/ICAM-1 interaction, such as compounds 18d and 18e with IC50 values of 110 and 70 nM, respectively. (C) 2002 Elsevier Science Ltd. All rights reserved.
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