A QSAR study of HIV protease inhibitors using theoretical descriptors.

Subhash C Basak, Denise Mills, Rajni Garg, Barun Bhhatarai

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

This paper reports the development of quantitative structure-activity relationship (QSAR) models for a set of 170 chemicals using mathematical descriptors which can be calculated directly from molecular structure without the input of any other experimental data. The calculated descriptors include topostructural (TS), topochemical (TC), and quantum chemical (QC). Because the situation is rank deficient i.e. the number of independent variables (descriptors) is larger than the number of compounds, three robust linear statistical modeling methods capable of handling such situations, viz., principal components regression (PCR), partial least square (PLS), and ridge regression (RR) were used for QSAR formulation. Results show that PLS and RR gave better q2 values as compared to the PCR method. Of the three classes of descriptors, the TC indices were the best predictors of anti-HIV activity and the QC indices were the least effective.

Original languageEnglish (US)
Pages (from-to)269-282
Number of pages14
JournalCurrent Computer-Aided Drug Design
Volume6
Issue number4
StatePublished - Dec 2010

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