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3D‐QSAR studies of cytotoxic heterocyclic quinones using calculated reduction potential
Author(s) -
Lee Yoonji,
Kim Seoeun,
Rhee HeeKyung,
Doh KyungEun,
Park Junhee,
Lee ChongOck,
Choi Sun,
Choo HeaYoung Park
Publication year - 2009
Publication title -
drug development research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.582
H-Index - 60
eISSN - 1098-2299
pISSN - 0272-4391
DOI - 10.1002/ddr.20320
Subject(s) - pharmacophore , chemistry , quantitative structure–activity relationship , stereochemistry , homo/lumo , intercalation (chemistry) , molecule , computational chemistry , organic chemistry
Most quinones with 2–4 fused aromatic rings exhibit cytostatic activity via DNA intercalation that causes enzyme blockade and reading errors during the replication process. The redox activity of quinones plays a role in the DNA cleavage mediated by oxygen or sulfur radicals. To develop novel anticancer agents based on nitrogen‐containing heterocyclic quinones, pharmacophore models of representative molecules with high activity were generated using Genetic Algorithm with Linear Assignment of Hypermolecular Alignment of Database (GALAHAD). A series of compounds were aligned to the selected pharmacophore model and the 3D‐quantitative structure activity relationships (QSAR) were analyzed using comparative molecular field analysis (CoMFA) and comparative molecular similarity indices analysis (CoMSIA), resulting in q 2 values of 0.734 and r 2 of 0.951, and q 2 of 0.803 and r 2 of 0.917, respectively, in each study. In addition, the potentials for the one‐electron reduction of quinones were calculated from LUMO energies using the semi‐empirical Austin Model 1 (AM1) method. These also showed a good correlation (r 2 of 0.816) with the cytotoxic activities of the quinones. Drug Dev Res 2009. © 2009 Wiley‐Liss, Inc.