Journal
JOURNAL OF THE TAIWAN INSTITUTE OF CHEMICAL ENGINEERS
Volume 59, Issue -, Pages 61-68Publisher
ELSEVIER
DOI: 10.1016/j.jtice.2015.07.024
Keywords
HIV-1 integrase enzyme; CoMFA; CoMSIA; Molecular docking; MOLCAD
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HIV integrase enzyme is well established potential target for antiretroviral therapy since a decade. Resistance to drugs (Raltegravir and Elvitegravir) used as HIV integrase inhibitors is already been identified and there is an urgent need to discover newer molecules which can overcome this issue. With this aim, ligand based drug design technique, 3D-QSAR, was carried out on a series of 5-hydroxy-6-oxo-1,6-dihydropyrimidine-4-carboxamide derivatives as HIV-1 integrase inhibitors. CoMFA and CoMSIA approaches were used for this study. The total dataset of 35 derivatives were divided into training set (28) and test set (7) in 80:20 ratio. In CoMFA model, the cross validated q(2) and the non-cross validated r(2) value for training set were found as 0.683 and 0.988, respectively; while in CoMSIA model, q(2) value was 0.707 and r(2) value was 0.989. Further the most active compound 3 was docked into binding site of integrase enzyme using SurFlex-Dock. The CoMFA and CoMSIA contour maps, MOLCAD-generated surface maps of binding site and docking poses were found complimentary with each other in terms of electrostatic, lipophilicity, and hydrogen-bonding potential. These results were used to design novel quinoxaline derivatives as HIV-1 integrase inhibitors which could be explore in future to identify novel HIV-1 integrase inhibitors. (C) 2015 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
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