2016
DOI: 10.1007/s00044-016-1745-1
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Identification of novel inhibitors of HCV NS3 protease genotype 3 subtype B through molecular docking studies of phytochemicals from Boerhavia diffusa L

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Cited by 3 publications
(1 citation statement)
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“…The in vitro molecular docking analysis by JunaBeegum et al (2017) to determine the potent inhibitory effect of recombinant NS3 genotype 3b catalytic activity of ethanolic extract of BD found that most flavonoids were deeply bound in HCV NS3 protease and interacted with the catalytic triad. The lead molecules liriodendrin, 3,5,6-tri-hydroxyl-4-methoxy flavone7-β-D glucoside, astragalin, caffeoyl tartaric acid, quercetin, 3,3,5,7-tetra-hydroxyl-4-methoxy flavones, boerhavin A, 4,25-secoobscurinervan and 3,5,7,2,5-penta-hydroxyl flavones had anti HCV activity.…”
Section: Methodsmentioning
confidence: 99%
“…The in vitro molecular docking analysis by JunaBeegum et al (2017) to determine the potent inhibitory effect of recombinant NS3 genotype 3b catalytic activity of ethanolic extract of BD found that most flavonoids were deeply bound in HCV NS3 protease and interacted with the catalytic triad. The lead molecules liriodendrin, 3,5,6-tri-hydroxyl-4-methoxy flavone7-β-D glucoside, astragalin, caffeoyl tartaric acid, quercetin, 3,3,5,7-tetra-hydroxyl-4-methoxy flavones, boerhavin A, 4,25-secoobscurinervan and 3,5,7,2,5-penta-hydroxyl flavones had anti HCV activity.…”
Section: Methodsmentioning
confidence: 99%