含1,2,4-三唑基团的新曼尼希碱的合成及其硅质抗高血压活性预后

L. Perekhoda, V. Georgiyants, H. Yeromina, I. Drapak, V. Lubenets, Z. Ieromina, I. Sych, H. Severina, A. Demchenko
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引用次数: 5

摘要

作为我们对morpholine和哌啶衍生物中潜在降压药物研究的一部分,我们设计合成了10个含有1,2,4-三唑和morpholine或哌啶基团的新型靶化合物,并进行对接研究,以寻找具有降压活性的生物活性物质。计算机研究表明,所有合成的化合物都是有前途的血管紧张素转换酶抑制剂,根据经合组织项目的化学物质分类,属于毒性4和5类。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Synthesis and In Silico Antihypertensive Activity Prognosis of New Mannich Bases Containing the 1,2,4-Triazole Moiety
As a part of our continuous research on potential antihypertensive agents among morpholine and piperidine derivatives, 10 novel target compounds containing 1,2,4-triazole and morpholine or piperidine moieties have been designed and synthesized, and the docking studies have been conducted in order to find biologically active substances with the antihypertensive activity. The in silico studies have shown that all compounds synthesized are promising angiotensin converting enzyme inhibitors and belong to the toxicity class 4 and 5 according to the classification of chemicals by the OECD project.
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