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QSAR with electrotopological state
atom index: human factor Xa inhibitor
N2-aroylanthranilamides.
Roy K, De AU, Sengupta
C.
Department of Pharmaceutical Technology, Jadavpur
University, Calcutta, India. [email protected]
Recently,
N2-aroylanthranilamides have been reported as novel series of possible
anticoagulant drug candidates and the two aryl rings (A and B) have been
suggested to interact with S1 and S4 regions, respectively, of human
factor Xa (hfXa). In the present effort, quantitative structure-activity
relationship (QSAR) of the hfXa binding affinity of 32
N2-aroylanthranilamides have been attempted, in continuation of our
previous report on the QSAR analysis of the data set using linear free
energy related (LFER) model, with electrotopological state atom (ETSA)
index (Kier and Hall, 1991, Adv. Drug Design., 22, 1-38), to explore the
atoms/regions of the compounds that modulate the activity comparatively
to the greater extent. The univariate and bivariate relations involving
the ETSA values of different common atoms of the compounds show
importance of the atom nos. 12, 3 and 17 (arbitrary numbering): B ring
carbon bearing meta R2 substituents, C ring carbon bearing R4
substituent, and carbonyl oxygen of A ring amide linkage. The importance
of atom 12 is suggested to be due to detrimental effects of meta R2
substituents (B ring) on the hfXa binding affinity, which may be owing
to interference in the attainment of the proper orientation of the
phenyl ring in the S4 site. Atom 3 signifies the impact of R4
substituents (central C ring) on the binding affinity. Again, atom 17
(carbonyl oxygen of A ring amide linkage) has been suggested to form
hydrogen bonding with the NH group of the other amide linkage, producing
a pseudo ring and thus stabilizing the structure. The relations were
improved further using indicator and physicochemical variables and the
present results are in good agreement with the previous findings of the
Hansch analysis.
PMID: 12375631 [PubMed - in process]
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