A 4D-QSAR study on anti-HIV HEPT analogues

被引:39
|
作者
Bak, A [1 ]
Polanski, J [1 ]
机构
[1] Silesian Univ, Inst Chem, Dept Organ Chem, PL-40006 Katowice, Poland
关键词
4D QSAR; SOM-4D-QSAR; anti-HIV; reverse transcriptase;
D O I
10.1016/j.bmc.2005.08.023
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
We used the 4D-QSAR method coupled with the PLS analysis and uninformative variable elimination or its variants for the investigations of the antiviral activity of HEPT, a series of conformationally flexible molecules that bind HIV-1 reverse transcriptase. An analysis of several Hopfinger's and SOM-4D-QSAR models indicated that both methods yield comparable results. Generally, charge descriptors provide better modeling efficiency. We have shown that the method properly indicates the mode of interaction revealed by X-ray Studies. It also allows us to calculate highly predictive QSAR models. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:273 / 279
页数:7
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