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- W2280104005 abstract "HIV-1 Protease (HIV-1 PR) enzymes are essential for accurate assembly and maturation of infectious HIV retroviruses. The significant role of HIV-1 protease in viral replication has made it a potential drug target. In the recent past, phytochemical Gallic Acid (GA) derivatives have been screened for protease inhibitor activity. The present work aims to design and evaluate potential GA-based HIV-1 PR phytoinhibitors by docking approach. The ligands were prepared by ChemDraw and docking was performed in HEX software. In this present study, one of the GA analogues (GA4) emerged as a potent drug candidate for HIV-1 PR inhibition, and docking results showed it to be comparable with anti-HIV drugs, darunavir and amprenavir. The GA4 derivative provided a lead for designing more effective HIV-1 PR inhibitors." @default.
- W2280104005 created "2016-06-24" @default.
- W2280104005 creator A5003891896 @default.
- W2280104005 creator A5029384299 @default.
- W2280104005 date "2015-01-01" @default.
- W2280104005 modified "2023-10-03" @default.
- W2280104005 title "Docking analysis of gallic acid derivatives as HIV-1 protease inhibitors" @default.
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- W2280104005 doi "https://doi.org/10.1504/ijbra.2015.073239" @default.
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