依那普利脯氨酸衍生物作为潜在的血管紧张素转换酶抑制剂。

Il Farmaco; edizione scientifica Pub Date : 1988-12-01
R Ciabatti, G Tarzia, F Battaglia, D Barone, E Baldoli
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引用次数: 0

摘要

报道了一类新的血管紧张素转换酶(ACE)抑制剂——依那普利类似物的合成。在这些分子中,依那普利的c端氨基酸序列Ala-Pro被Pro-Pro序列取代。在体外和体内对这些化合物进行了测试。它们在体内没有活性,但只有一周的体外抑制活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prolyl derivatives of enalapril as potential angiotensin converting enzyme inhibitors.

The synthesis of a new class of potential angiotensin converting enzyme (ACE) inhibitors, analogs of enalapril, is reported. In these molecules the C-terminal amino acidic sequence Ala-Pro of enalapril was replaced by the sequence Pro-Pro. The compounds were tested both in vitro and in vivo. They showed no in vivo activity but only a week in vitro inhibitory activity.

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