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Bulletin of the Korean Chemical Society (BKCS)

ISSN 0253-2964(Print)
ISSN 1229-5949(Online)
Volume 32, Number 1
BKCSDE 32(1)
January 20, 2011

Title	Investigation of the binding affinity between styrylquinoline inhibitors and HIV integrase using calculated nuclear quadrupole coupling constant (NQCC) parameters (A theoretical ab initio study)
Author	Marjan A. Rafiee*, Tayyebe Partoee
Keywords	AIDS, Charge density, HIV, NQR, Styrylquinoline
Abstract	In this work, the calculated nuclear quadrupole coupling constants of ¹⁷O in some styrylquinoline conformers were presented. The calculations were carried out to find the relationships between the charge distribution of styrylquinolines and their pharmaceutical behavior and to explore the differences among the electronic structures of some conformers of these potent HIV IN inhibitors. Furthermore, the HIV IN inhibitory of R1 and R2 rotamers was compared. On the basis of our results: - Charge density on oxygen atoms of carboxyl moiety has a dominant role in the drug activity. - The a conformer in which a divalent hydrogen atom is a link, has more capability in antiviral drug treatment. - The R1 conformer, as a Mg⁺² chelating agent, is better than R2 conformer and thus it is more inhibitor of HIV IN.
Page	208 - 212
Full Text	PDF

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