Title of article
Understanding the antifungal activity of terbinafine analogues using quantitative structure–activity relationship (qsar) models Original Research Article
Author/Authors
Vijay M Gokhale، نويسنده , , Vithal M Kulkarni، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2000
Pages
13
From page
2487
To page
2499
Abstract
Terbinafine and its analogues, which are a major class of non-azole antifungal agents, are known to act by inhibition of squalene epoxidase enzyme in fungal cells. We have performed a quantitative structure–activity relationship (QSAR) study on a series of 92 molecules using different types of physicochemical descriptors. Inhibitors were divided into five classes depending upon chemical structure. QSAR models were generated for correlation between antifungal activity against Candida albicans using genetic function approximation (GFA) technique. Equations were evaluated using internal as well as external test set predictions. Models generated for all these classes show that steric properties and conformational rigidity of side chains play an important role for the activity. The present QSAR analysis agrees with the results of the previously reported CoMFA study.
Journal title
Bioorganic and Medicinal Chemistry
Serial Year
2000
Journal title
Bioorganic and Medicinal Chemistry
Record number
1301236
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