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An extensive ecdysteroid CoMFA
Authors:Laurence Dinan  Robert E Hormann  Ted Fujimoto
Institution:(1) Department of Biological Sciences, University of Exeter, Perry Road, Exeter, EX4 4QG, U.K;(2) 727 Norristown Road, Spring House, PA , 19477-0904, U.S.A
Abstract:The ecdysteroid agonist activity of 71 HPLC-purified ecdysteroids was measured in the Drosophila melanogaster BII tumorous blood cell line assay. The resultant log(ED50) values, spanning almost 6 orders of magnitude, were used to construct a comparative molecular field analysis (CoMFA) model in which conformations were selected by homology to the crystal structure of ecdysone. Model A was constructed by utilization of the region- focused electrostatic indicator field (q2=0.631, r2=0.903, 5 components, 4 outliers). Model B made use of region-focused electrostatic and steric indicator fields along with MlogP (q2=0.694, r2=0.892, 5 components, 4 outliers). The model and its underlying bioassay data support a pharmacophore hypothesis in which ecdysteroid binding is understood to be due principally to the summation of localized interactions from approximately six specific loci. This is in contrast to previous structure-activity relationship hypotheses which are formulated in terms of the presence or absence of essential functional groups, without which ecdysteroid receptor affinity would be completely absent. The present CoMFA model is utilized to predict the activities of heretofore unknown ecdysteroids.
Keywords:CoMFA  3D QSAR  ecdysone  ecdysteroid  ligand-binding  receptor
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