Quantitative Structure−Activity Relationship (5D-QSAR) Study of Combretastatin-like Analogues as Inhibitors of Tubulin Assembly

A molecular modeling study was carried out to develop a predictive model for combretastatin-like analogues populating the colchicine-binding site of β-tubulin. A series of compounds built around a framework including two aromatic groups linked by various moieties such as alkenes (stilbenes), enones...

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Veröffentlicht in:Journal of medicinal chemistry 2005-01, Vol.48 (2), p.457-465
Hauptverfasser: Ducki, Sylvie, Mackenzie, Grant, Lawrence, Nicholas J, Snyder, James P
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container_title Journal of medicinal chemistry
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creator Ducki, Sylvie
Mackenzie, Grant
Lawrence, Nicholas J
Snyder, James P
description A molecular modeling study was carried out to develop a predictive model for combretastatin-like analogues populating the colchicine-binding site of β-tubulin. A series of compounds built around a framework including two aromatic groups linked by various moieties such as alkenes (stilbenes), enones (chalcones), or ethers was selected for the study. The 5D-QSAR model was developed stepwise. First a model was generated for the chalcone series (19 compounds, 71 conformations), then for the stilbene series (18 compounds, 59 conformations), and finally for the combined dataset (47 ligands, 160 conformers). Although the models for the chalcone and stilbene series appeared slightly different when represented by QSAR colored surfaces, the combined model seems to reconcile the differences without compromise and represents a highly predictive model for compounds that bind to the colchicine-binding site of tubulin.
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subjects Antineoplastic Agents - chemistry
Bibenzyls - chemistry
Binding Sites
Colchicine - chemistry
Ligands
Models, Molecular
Molecular Conformation
Monte Carlo Method
Quantitative Structure-Activity Relationship
Stilbenes - chemistry
Tubulin - chemistry
Tubulin Modulators
title Quantitative Structure−Activity Relationship (5D-QSAR) Study of Combretastatin-like Analogues as Inhibitors of Tubulin Assembly
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