酶
血管紧张素转换酶
化学
肾素-血管紧张素系统
药理学
功能(生物学)
血压
血管紧张素II
生物化学
内科学
医学
生物
细胞生物学
受体
作者
Arthur A. Patchett,Elbert E. Harris,Edward W. Tristram,Matthew J. Wyvratt,Mingshu Wu,D. Taub,Elwood R. Peterson,Theodore J. Ikeler,J. ten Broeke,L. G. Payne,Debra L. Ondeyka,Eugene D. Thorsett,W. J. GREENLEE,Nancy S. Lohr,R. D. Hoffsommer,H Joshua,W. V. Ruyle,John W. Rothrock,Susan D. Aster,Alan L. Maycock
出处
期刊:Nature
[Nature Portfolio]
日期:1980-11-01
卷期号:288 (5788): 280-283
被引量:707
摘要
Much current attention focuses on the renin–angiotensin system in relation to mechanisms controlling blood pressure and renal function. Recent demonstrations (ref 1, ref. 2 and refs therein) that angiotensin-converting enzyme inhibitors show promising clinical antihypertensive properties have been of particular interest. We now report on the design of a novel series of substituted N-carboxymethyl-dipeptides which are active in inhibiting angiotensin-converting enzyme at nanomolar levels. We suggest that these compounds are transition-state inhibitors and that extensions of this design to other metalloendopeptidases merit further study.
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