Annals of Antivirals and Antiretrovirals

    Abstract

    Open Access Research Article Article ID: AAA-2-103

    Thiolutin Derivatives as inhibitor of RNA-Dependent RNA Polymerase (RdRP) of Hepatitis C Virus: An In-silico Approach

    Muhammad Imran Qadir*, Asma Munawar, Syed Bilal Hussain

    Docking study of few Thiolutin derivatives, which originally act as Hepatitis C Virus RNA Dependent RNA Polymerase (RdRP) inhibitor, was performed by using AutoDock Vina. The docking studies reveal that thiolutin interacted with Hepatitis C Virus RNA Dependent RNA Polymerase through hydrogen bonding as well as hydrophobic interactions. Its binding energy after modification (Thiolutin1) was -6.7 kcal/mol, which was greater than the original thiolutin affinity.

    Keywords: Thiolutin; Drug design; Hydrogen bonding; Hepatitis C Virus RNA Dependent RNA Polymerase; AutoDock Vina

    Published on: Jan 17, 2018 Pages: 1-3

    Full Text PDF Full Text HTML DOI: 10.17352/aaa.000003
    Get Citation Base Search Scilit OAI-PMH ResearchGate GrowKudos CrossMark

    Global Views

    Case Reports

    Peertechz Tweets

    Pinterest on AAA