Current time in Korea 20:19 Nov 25 (Sat) Year 2017 KCS KCS Publications
KCS Publications
My Journal Log In Register
HOME > Search > Browsing(BKCS) > Archives

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