期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 12, 期 9, 页码 1275-1278出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0960-894X(02)00149-X
关键词
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A novel non-peptidyl endothelin converting enzyme inhibitor was obtained through a pharmacophore analysis of known inhibitors and three-dimensional structure database search. Analogues of the new inhibitor were designed using the structure-activity relationship of known inhibitors and synthesized. In anesthetized rats, intraperitoneal administration of the analogues suppressed the pressor responses induced by big endothelin-1. (C) 2002 Elsevier Science Ltd. All rights reserved.
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