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 |
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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. |
doi_str_mv | 10.1021/jm049444m |
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Med. Chem</addtitle><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.</description><subject>Antineoplastic Agents - chemistry</subject><subject>Bibenzyls - chemistry</subject><subject>Binding Sites</subject><subject>Colchicine - chemistry</subject><subject>Ligands</subject><subject>Models, Molecular</subject><subject>Molecular Conformation</subject><subject>Monte Carlo Method</subject><subject>Quantitative Structure-Activity Relationship</subject><subject>Stilbenes - chemistry</subject><subject>Tubulin - chemistry</subject><subject>Tubulin Modulators</subject><issn>0022-2623</issn><issn>1520-4804</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0MtuEzEUBmALgWhaWPACaDagdjHg64xnOUpLU6kSbRJgadkTmzqdGQdfEFmyY80j9knqKFHZsLEln0__sX4A3iD4AUGMPq4HSBtK6fAMTBDDsKQc0udgAiHGJa4wOQLHIawhhARh8hIcIVYxzlkzAb9vkxyjjTLan7pYRJ-6mLx--PO37fKTjdtirvs8dWO4s5vilJ2Xt4t2fpZtWm0LZ4qpG5TXUYZdyFj29l4X7Sh79z3pUMhQXI13VtnofNjxZVKpt2PRhqAH1W9fgRdG9kG_Ptwn4Muni-V0Vl5_vryattelJLyKpakaXtVwxRln-aBd0xhomhWrCeugYpgjKKVSiBKoqEGKQl5rqEhtMK2wISfg_T53492P_LMoBhs63fdy1C4FUdWkQpzWGZ7tYeddCF4bsfF2kH4rEBS7vsVT39m-PYQmNejVP3koOINyD2yI-tfTXPr73cKaieXNQsyam8tvdPZVzLN_t_eyC2Ltks9Fhv8sfgRzlpgr</recordid><startdate>20050127</startdate><enddate>20050127</enddate><creator>Ducki, Sylvie</creator><creator>Mackenzie, Grant</creator><creator>Lawrence, Nicholas J</creator><creator>Snyder, James P</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20050127</creationdate><title>Quantitative Structure−Activity Relationship (5D-QSAR) Study of Combretastatin-like Analogues as Inhibitors of Tubulin Assembly</title><author>Ducki, Sylvie ; Mackenzie, Grant ; Lawrence, Nicholas J ; Snyder, James P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a386t-f698670d8585d854c99f0f9d5735c0b52810aabb1430b4f1b4087e0b37f2462f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Antineoplastic Agents - chemistry</topic><topic>Bibenzyls - chemistry</topic><topic>Binding Sites</topic><topic>Colchicine - chemistry</topic><topic>Ligands</topic><topic>Models, Molecular</topic><topic>Molecular Conformation</topic><topic>Monte Carlo Method</topic><topic>Quantitative Structure-Activity Relationship</topic><topic>Stilbenes - chemistry</topic><topic>Tubulin - chemistry</topic><topic>Tubulin Modulators</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ducki, Sylvie</creatorcontrib><creatorcontrib>Mackenzie, Grant</creatorcontrib><creatorcontrib>Lawrence, Nicholas J</creatorcontrib><creatorcontrib>Snyder, James P</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ducki, Sylvie</au><au>Mackenzie, Grant</au><au>Lawrence, Nicholas J</au><au>Snyder, James P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative Structure−Activity Relationship (5D-QSAR) Study of Combretastatin-like Analogues as Inhibitors of Tubulin Assembly</atitle><jtitle>Journal of medicinal chemistry</jtitle><addtitle>J. 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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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