Topological designing of 4-piperazinylquinazolines as antagonists of PDGFR tyrosine kinase family.

Abstract Topological designing of a series of 4-piperazinylquinazolines as antagonists of platelet-derived growth factor receptor (PDGFR) tyrosine kinase family has been reported using a series of distance-based topological indices. Regression analysis of the data, using maximum R 2 method indicated that inhibitory activity, pIC 50 (μm), in cellular PGDFR phosphorylation assay can be modelled excellently in multi-parametric model. The results are discussed critically using cross-validated parameters.