An extensive ecdysteroid CoMFA

被引:76
作者
Dinan, L
Hormann, RE
Fujimoto, T
机构
[1] Rohm & Haas Co, Spring House, PA 19477 USA
[2] Univ Exeter, Dept Sci Biol, Exeter EX4 4QG, Devon, England
关键词
CoMFA; 3D QSAR; ecdysone; ecdysteroid; ligand-binding; receptor;
D O I
10.1023/A:1008052320014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ecdysteroid agonist activity of 71 HPLC-purified ecdysteroids was measured in the Drosophila melanogaster B-II 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 (q(2) = 0.631, r(2) = 0.903, 5 components, 4 outliers). Model B made use of region-focused electrostatic and steric indicator fields along with MlogP (q(2) = 0.694, r(2) = 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.
引用
收藏
页码:185 / 207
页数:23
相关论文
共 52 条
[51]  
1996, SYBYL LIGAND BASED M, P64
[52]  
1996, SYBYL LIGAND BASED D, P78