Three-dimensional quantitative structure-activity relationship analyses   of a series of butenolide ETA antagonists

CORC > 北京大学 > 化学与分子工程学院

	Three-dimensional quantitative structure-activity relationship analyses of a series of butenolide ETA antagonists
	Zhu, LL ; Xu, XJ
刊名	中国化学英文版
	2003
关键词	CoMFA CoMSIA 3D-QSAR butenolide ETA selective antagonists all-space search MOLECULAR SIMILARITY INDEXES HYDROGEN-BONDING PROPERTIES SMOOTH-MUSCLE CONTRACTION ENDOTHELIN RECEPTOR FIELD ANALYSIS ANALYSIS COMSIA CLONING POTENT CDNA EXPRESSION
英文摘要	Two kinds of Three-dimensional Quantitative Structure-activity Relationship (3D-QSAR) methods, comparative molecular field analysis (CoNWA) and comparative molecular similarity indices analysis (CoMSIA), were applied to analyze the structure-activity relationship of a series of 63 butenolkle ETA selective antagonists with respect to thew inhibition against human ETA receptor. The CoNWA and CoMSIA models were developed for the conceivable alignment of the molecules based on a template structure from the crystallized data. The statistical results from the initial orientation of the aligned molecules show that the 3D-QSAR model from CoNWA ( q(2) = 0.543) is Obviously Superior to that from the Conventional CoMSIA (q(2) = 0.407). In order to refine the model, all-space search (ASS) was applied to minimize the field sampling process. By rotating and translating the molecular aggregate within the grid systematically, all the possible samplings of the molecular fields were tested and subsequently the one with the highest q(2) was picked out. The comparison of the sensitivity of CoMFA and CoMSIA to different space orientation shows that the CoMFA q(2) Values are more sensitive to the translations and rotations of the aligned molecules with respect to the lattice than those of CoMSIA. The best CoMFA model from ASS was further refined by the region focused technique. The high quality of the best model is indicated by the high cross-validated correlation and the prediction on the external test set. The CoMFA coefficient contour plots identify several key features dud explain the wide range of activities, which may help us to design new effective ETA selective antagonists.; Chemistry, Multidisciplinary; SCI(E); 2; ARTICLE; 3; 261-269; 21
语种	英语
内容类型	期刊论文
源URL	[http://ir.pku.edu.cn/handle/20.500.11897/400831]
专题	化学与分子工程学院
推荐引用方式 GB/T 7714	Zhu, LL,Xu, XJ. Three-dimensional quantitative structure-activity relationship analyses of a series of butenolide ETA antagonists[J]. 中国化学英文版,2003.
APA	Zhu, LL,&Xu, XJ.(2003).Three-dimensional quantitative structure-activity relationship analyses of a series of butenolide ETA antagonists.中国化学英文版.
MLA	Zhu, LL,et al."Three-dimensional quantitative structure-activity relationship analyses of a series of butenolide ETA antagonists".中国化学英文版 (2003).