QSAR aspects of flavonoids as a plentiful source of new drugs.

The continuous raise of molecular diversity requires to find a guidelines for orientation it this. A likely occasion for consideration of new QSAR approach possibilities for this aspect is the flavonoids (F) multitude, the class of organic compounds (C) with very varied chemistry and pharmacology. The list of F affinities includes benzodiazepines, adenosine, estrogen receptors and row of enzymes phosphodiesterase, proteinthyrosine kinase, aromatase, xanthine oxidase asf.