甲基噻吩啉酚类化合物(LQM300系列)与血管紧张素转换酶(ACE)对接研究。

Q2 Pharmacology, Toxicology and Pharmaceutics Open Medicinal Chemistry Journal Pub Date : 2013-11-23 eCollection Date: 2013-01-01 DOI:10.2174/1874104501307010030
Víctor H Vázquez-Valadez, V H Abrego, Pablo A Martínez, Gabriela Torres, Oscar Zúñiga, Daniel Escutia, Rebeca Vilchis, Ana Ma Velázquez, Luisa Martínez, Mónica Ruiz, Brígida Camacho, Rafael López-Castañares, Enrique Angeles
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引用次数: 7

摘要

治疗高血压的主要靶点是血管紧张素转换酶(ACE)。这种酶负责产生血管紧张素II,一种有效的血管收缩剂。因此,抑制ACE活性是治疗高血压的靶点之一。因此,本研究的目的是利用计算研究来证明所提出的杂环化合物对ACE具有分子亲和力,此外,这些杂环化合物能够抑制ACE活性,从而避免血管加压素II的产生。所有这些都是通过计算机辅助药物设计,研究系统,通过分子识别过程,并与市场上已有的高血压化合物进行比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Docking Studies of Methylthiomorpholin Phenols (LQM300 Series) with Angiotensin-Converting Enzyme (ACE).

A main target in the treatment of hypertension is the angiotensin-converting enzyme (ACE). This enzyme is responsible for producing angiotensin II, a potent vasoconstrictor. Therefore, one of the targets in the treatment of hypertension is to inhibit ACE activity. Hence, this study's aim is to use computational studies to demonstrate that the proposed heterocyclic compounds have a molecular affinity for ACE and that, furthermore, these heterocyclic compounds are capable of inhibiting ACE activity, thus avoiding the production of the vasopressor Angiotensin II. All this using computer-aided drug design, and studying the systems, with the proposed compounds, through molecular recognition process and compared with the compounds already on the market for hypertension.

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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
自引率
0.00%
发文量
4
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