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印度尼西亚草药数据库作为HIV-1逆转录酶抑制剂的虚拟筛选

Virtual screening of Indonesian herbal database as HIV-1 reverse transcriptase inhibitor.

作者信息

Syahdi Rezi Riadhi, Mun'im Abdul, Suhartanto Heru, Yanuar Arry

机构信息

Faculty of Pharmacy, University of Indonesia, Depok 16424, Indonesia.

出版信息

Bioinformation. 2012;8(24):1206-10. doi: 10.6026/97320630081206. Epub 2012 Dec 8.

Abstract

HIV-1 (Human immunodeficiency virus type 1) is a member of retrovirus family that could infect human and causing AIDS disease. AIDS epidemic is one of most destructive diseases in modern era. There were more than 33 million people infected by HIV until 2010. Various studies have been widely employed to design drugs that target the essential enzymes of HIV-1 that is, reverse transcriptase, protease and integrase. In this study, in silico virtual screening approach is used to find lead molecules from the library or database of natural compounds as HIV-1 reverse transcriptase inhibitor. Virtual screening against Indonesian Herbal Database using AutoDock4 performed on HIV-1 reverse transcriptase. From the virtual screening, top ten compounds were mulberrin, plucheoside A, vitexilactone, brucine N-oxide, cyanidin 3-arabinoside, alpha-mangostin, guaijaverin, erycristagallin, morusin and sanggenol N.

摘要

HIV-1(人类免疫缺陷病毒1型)是逆转录病毒家族的成员,可感染人类并导致艾滋病。艾滋病流行是现代最具破坏性的疾病之一。截至2010年,超过3300万人感染了艾滋病毒。各种研究已广泛用于设计针对HIV-1关键酶(即逆转录酶、蛋白酶和整合酶)的药物。在本研究中,采用计算机虚拟筛选方法从天然化合物库或数据库中寻找作为HIV-1逆转录酶抑制剂的先导分子。使用AutoDock4对印度尼西亚草药数据库进行针对HIV-1逆转录酶的虚拟筛选。从虚拟筛选中,排名前十的化合物是桑色素、羽扇豆苷A、牡荆内酯、马钱子碱N-氧化物、花青素3-阿拉伯糖苷、α-山竹黄酮、槐属苷、刺桐素、桑辛素和桑根醇N。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe1/3530873/b47bac46bf96/97320630081206F1.jpg

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