期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 13, 期 13, 页码 2101-2104出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0960-894X(03)00404-9
关键词
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The parallel synthesis of novel inhibitors of procollagen C-terminal proteinase is described. The synthetic strategy allowed for the facile synthesis of a large number of side-chain diversified diamino acid hydroxamates, of which the D-diaminopropionic acid derivatives were shown to be single digit nanomolar PCP inhibitors. (C) 2003 Elsevier Science Ltd. All rights reserved.
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