Suppr超能文献

可可树(Theobroma cacao L.)化合物:作为主要SARS-CoV-2蛋白酶抑制剂的理论研究与分子建模

Theobroma cacao L. compounds: Theoretical study and molecular modeling as inhibitors of main SARS-CoV-2 protease.

作者信息

Yañez Osvaldo, Osorio Manuel Isaías, Areche Carlos, Vasquez-Espinal Alejandro, Bravo Jessica, Sandoval-Aldana Angélica, Pérez-Donoso José M, González-Nilo Fernando, Matos Maria João, Osorio Edison, García-Beltrán Olimpo, Tiznado William

机构信息

Computational and Theoretical Chemistry Group, Departamento de Ciencias Químicas, Facultad de Ciencias Exactas, Universidad Andres Bello, República 498, Santiago, Chile; Center of New Drugs for Hypertension (CENDHY), Santiago, Chile; Department of Pharmaceutical Science and Technology, School of Chemical and Pharmaceutical Sciences, Universidad de Chile, Santiago, Chile.

Facultad de Medicina, Centro de Investigación Biomédica, Universidad Diego Portales, Ejército 141, Santiago 837007, Chile; Center for Bioinformatics and Integrative Biology (CBIB), Facultad de Ciencias de la Vida, Universidad Andres Bello, Av. República 330, Santiago 8370146, Chile.

出版信息

Biomed Pharmacother. 2021 Aug;140:111764. doi: 10.1016/j.biopha.2021.111764. Epub 2021 May 24.

Abstract

Cocoa beans contain antioxidant molecules with the potential to inhibit type 2 coronavirus (SARS-CoV-2), which causes a severe acute respiratory syndrome (COVID-19). In particular, protease. Therefore, using in silico tests, 30 molecules obtained from cocoa were evaluated. Using molecular docking and quantum mechanics calculations, the chemical properties and binding efficiency of each ligand was evaluated, which allowed the selection of 5 compounds of this series. The ability of amentoflavone, isorhoifolin, nicotiflorin, naringin and rutin to bind to the main viral protease was studied by means of free energy calculations and structural analysis performed from molecular dynamics simulations of the enzyme/inhibitor complex. Isorhoifolin and rutin stand out, presenting a more negative binding ΔG than the reference inhibitor N-[(5-methylisoxazol-3-yl)carbonyl]alanyl-l-valyl-N1-((1R,2Z)-4-(benzyloxy)-4-oxo-1-{[(3R)-2-oxopyrrolidin-3-yl]methyl}but-2-enyl)-L-leucinamide (N3). These results are consistent with high affinities of these molecules for the major SARS-CoV-2. The results presented in this paper are a solid starting point for future in vitro and in vivo experiments aiming to validate these molecules and /or test similar substances as inhibitors of SARS-CoV-2 protease.

摘要

可可豆含有具有抑制2型冠状病毒(SARS-CoV-2)潜力的抗氧化分子,该病毒会引发严重急性呼吸综合征(COVID-19)。特别是蛋白酶。因此,通过计算机模拟测试,对从可可中获得的30种分子进行了评估。利用分子对接和量子力学计算,评估了每个配体的化学性质和结合效率,从而从该系列中筛选出5种化合物。通过对酶/抑制剂复合物进行分子动力学模拟并进行自由能计算和结构分析,研究了穗花杉双黄酮、异荭草苷、烟花苷、柚皮苷和芦丁与主要病毒蛋白酶结合的能力。异荭草苷和芦丁表现突出,其结合自由能ΔG比参考抑制剂N-[(5-甲基异恶唑-3-基)羰基]丙氨酰-L-缬氨酰-N1-((1R,2Z)-4-(苄氧基)-4-氧代-1-{[(3R)-2-氧代吡咯烷-3-基]甲基}丁-2-烯基)-L-亮氨酰胺(N3)更负。这些结果与这些分子对主要SARS-CoV-2的高亲和力一致。本文给出的结果是未来旨在验证这些分子和/或测试类似物质作为SARS-CoV-2蛋白酶抑制剂的体外和体内实验的坚实起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d2c/8141698/1d66c4f534ae/gr1_lrg.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验