Vázquez-Valadez Víctor H, Abrego V H, Martínez Pablo A, Torres Gabriela, Zúñiga Oscar, Escutia Daniel, Vilchis Rebeca, Velázquez Ana Ma, Martínez Luisa, Ruiz Mónica, Camacho Brígida, López-Castañares Rafael, Angeles Enrique
Laboratorio de Química Medicinal, Departamento de C. Químicas FESC-Universidad Nacional Autónoma de México, Facultad de Química Universidad Autónoma del Estado de México.
Open Med Chem J. 2013 Nov 23;7:30-8. doi: 10.2174/1874104501307010030. eCollection 2013.
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.
高血压治疗的一个主要靶点是血管紧张素转换酶(ACE)。这种酶负责生成血管紧张素II,一种强效血管收缩剂。因此,高血压治疗的目标之一是抑制ACE活性。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,而且,这些杂环化合物能够抑制ACE活性,从而避免血管升压素血管紧张素II的产生。所有这些均通过计算机辅助药物设计来实现,并通过分子识别过程研究含有所提出化合物的系统,并与市场上已有的高血压治疗化合物进行比较。