Improved quantitative structure-activity relationship models to predict antioxidant activity of flavonoids in chemical, enzymatic, and cellular systems

Andrey Ivanovich Khlebnikov, Igor A. Schepetkin, Nina G. Domina, Liliya N. Kirpotina, Mark T. Quinn

Research output: Contribution to journalArticle

92 Citations (Scopus)

Abstract

Quantitative structure-activity relationship (QSAR) models are useful in understanding how chemical structure relates to the biological activity of natural and synthetic chemicals and for design of newer and better therapeutics. In the present study, 46 flavonoids and related polyphenols were evaluated for direct/indirect antioxidant activity in three different assay systems of increasing complexity (chemical, enzymatic, and intact phagocytes). Based on these data, two different QSAR models were developed using (i) physicochemical and structural (PC&S) descriptors to generate multiparameter partial least squares (PLS) regression equations derived from optimized molecular structures of the tested compounds and (ii) a partial 3D comparison of the 46 compounds with local fingerprints obtained from fragments of the molecules by the frontal polygon (FP) method. We obtained much higher QSAR correlation coefficients (r) for flavonoid end-point antioxidant activity in all three assay systems using the FP method (0.966, 0.948, and 0.965 for datasets evaluated in the biochemical, enzymatic, and whole cell assay systems, respectively). Furthermore, high leave-one-out cross-validation coefficients (q2) of 0.907, 0.821, and 0.897 for these datasets, respectively, indicated enhanced predictive ability and robustness of the model. Using the FP method, structural fragments (submolecules) responsible for the end-point antioxidant activity in the three assay systems were also identified. To our knowledge, this is the first QSAR model derived for description of flavonoid direct/indirect antioxidant effects in a cellular system, and this model could form the basis for further drug development of flavonoid-like antioxidant compounds with therapeutic potential.

Original languageEnglish
Pages (from-to)1749-1770
Number of pages22
JournalBioorganic and Medicinal Chemistry
Volume15
Issue number4
DOIs
Publication statusPublished - 15 Feb 2007
Externally publishedYes

Fingerprint

Quantitative Structure-Activity Relationship
Flavonoids
Antioxidants
Assays
Dermatoglyphics
Polyphenols
Phagocytes
Bioactivity
Molecular Structure
Least-Squares Analysis
Molecular structure
Molecules
Therapeutics
Pharmaceutical Preparations

Keywords

  • Antioxidants
  • Drug design
  • Flavonoids
  • Frontal polygons
  • Molecular descriptors
  • Phagocytes
  • Quantitative structure-activity relationship analysis
  • Reactive oxygen species

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Organic Chemistry
  • Drug Discovery
  • Pharmaceutical Science

Cite this

Improved quantitative structure-activity relationship models to predict antioxidant activity of flavonoids in chemical, enzymatic, and cellular systems. / Khlebnikov, Andrey Ivanovich; Schepetkin, Igor A.; Domina, Nina G.; Kirpotina, Liliya N.; Quinn, Mark T.

In: Bioorganic and Medicinal Chemistry, Vol. 15, No. 4, 15.02.2007, p. 1749-1770.

Research output: Contribution to journalArticle

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