具有潜在抗登革病毒活性的肉桂酸酰胺衍生物分子对接及动力学研究

IF 2.5 4区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Luis Alfonso Cárdenas-Granados, Manuel Alejandro Hernández-Serda, Omar Joel Villegas-Solís, Víctor Hugo Vázquez-Valadez, Aldo Yoshio Alarcón-López, Pablo A Martínez-Soriano, Jaqueline Ramos-Sánchez, Tannya Karen Castro-Jiménez, José Bustos-Arriaga, Enrique Angeles
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引用次数: 0

摘要

登革热被列为一种被忽视的热带病,由伊蚊传播,仍然是一项重大的全球卫生挑战,往往演变成出血热等严重的临床表现。尽管其影响广泛,但迄今为止尚未批准抗病毒治疗,这突出表明迫切需要有效和可获得的治疗方案。在目前的工作中,计算分析是在一个容易合成的咖啡酸苯乙酯类似物的内部文库中进行的,这些类似物对病毒包膜(E)蛋白具有潜在的活性,E蛋白是登革热病毒进入和膜融合的关键介质。其中,在分子动力学模拟中,LQM778在蛋白质-配体复合物内表现出一致的稳定性。这一发现为体外研究和未来的结构优化提供了基础,可能会改变登革热抗病毒药物开发的格局。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
"Molecular Docking and Dynamic Studies of Amide Derivatives from Cinnamic Acid with Potential Anti-Dengue Virus Activity".

Dengue, classified as a neglected tropical disease and transmitted by Aedes mosquitoes, remains a significant global health challenge, often evolving into severe clinical manifestations such as hemorrhagic fever. Despite its widespread impact, no antiviral therapy has been approved to date, highlighting the urgent need for effective and accessible treatment options. In the present work, computational analysis is performed on an in-house library of easily synthesized caffeic acid phenethyl ester analogs, which exhibit potential activity against the viral envelope (E) protein, a critical mediator of dengue virus entry and membrane fusion. Among them, LQM778 demonstrated consistent stability within the protein-ligand complex during molecular dynamics simulations. This finding provides a foundation for in vitro studies and future structural optimizations that could transform the landscape of antiviral development against dengue.

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来源期刊
ChemistryOpen
ChemistryOpen CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
4.80
自引率
4.30%
发文量
143
审稿时长
1 months
期刊介绍: ChemistryOpen is a multidisciplinary, gold-road open-access, international forum for the publication of outstanding Reviews, Full Papers, and Communications from all areas of chemistry and related fields. It is co-owned by 16 continental European Chemical Societies, who have banded together in the alliance called ChemPubSoc Europe for the purpose of publishing high-quality journals in the field of chemistry and its border disciplines. As some of the governments of the countries represented in ChemPubSoc Europe have strongly recommended that the research conducted with their funding is freely accessible for all readers (Open Access), ChemPubSoc Europe was concerned that no journal for which the ethical standards were monitored by a chemical society was available for such papers. ChemistryOpen fills this gap.
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