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A structure-based design of new C2- and C13-substituted taxanes: tubulin binding affinities and extended quantitative structure-activity relationships using comparative binding energy (COMBINE) analysis.

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Title: A structure-based design of new C2- and C13-substituted taxanes: tubulin binding affinities and extended quantitative structure-activity relationships using comparative binding energy (COMBINE) analysis.
Authors: Coderch C; Área de Farmacología, Departamento de Ciencias Biomédicas, Universidad de Alcalá, E-28871 Alcalá de Henares, Unidad Asociada al Instituto de Química Médica del CSIC, Madrid, Spain., Tang Y, Klett J, Zhang SE, Ma YT, Shaorong W, Matesanz R, Pera B, Canales A, Jiménez-Barbero J, Morreale A, Díaz JF, Fang WS, Gago F
Source: Organic & biomolecular chemistry [Org Biomol Chem] 2013 May 14; Vol. 11 (18), pp. 3046-56.
Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 101154995 Publication Model: Print Cited Medium: Internet ISSN: 1477-0539 (Electronic) Linking ISSN: 14770520 NLM ISO Abbreviation: Org Biomol Chem Subsets: MEDLINE
Database: MEDLINE Ultimate
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An: 23532250
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PubType: Academic Journal
PubTypeId: academicJournal
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  Data: A structure-based design of new C2- and C13-substituted taxanes: tubulin binding affinities and extended quantitative structure-activity relationships using comparative binding energy (COMBINE) analysis.
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  Data: <searchLink fieldCode="AU" term="%22Coderch+C%22">Coderch C</searchLink>; Área de Farmacología, Departamento de Ciencias Biomédicas, Universidad de Alcalá, E-28871 Alcalá de Henares, Unidad Asociada al Instituto de Química Médica del CSIC, Madrid, Spain.<br /><searchLink fieldCode="AU" term="%22Tang+Y%22">Tang Y</searchLink><br /><searchLink fieldCode="AU" term="%22Klett+J%22">Klett J</searchLink><br /><searchLink fieldCode="AU" term="%22Zhang+SE%22">Zhang SE</searchLink><br /><searchLink fieldCode="AU" term="%22Ma+YT%22">Ma YT</searchLink><br /><searchLink fieldCode="AU" term="%22Shaorong+W%22">Shaorong W</searchLink><br /><searchLink fieldCode="AU" term="%22Matesanz+R%22">Matesanz R</searchLink><br /><searchLink fieldCode="AU" term="%22Pera+B%22">Pera B</searchLink><br /><searchLink fieldCode="AU" term="%22Canales+A%22">Canales A</searchLink><br /><searchLink fieldCode="AU" term="%22Jiménez-Barbero+J%22">Jiménez-Barbero J</searchLink><br /><searchLink fieldCode="AU" term="%22Morreale+A%22">Morreale A</searchLink><br /><searchLink fieldCode="AU" term="%22Díaz+JF%22">Díaz JF</searchLink><br /><searchLink fieldCode="AU" term="%22Fang+WS%22">Fang WS</searchLink><br /><searchLink fieldCode="AU" term="%22Gago+F%22">Gago F</searchLink>
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  Data: <searchLink fieldCode="JN" term="%22101154995%22">Organic & biomolecular chemistry</searchLink> [Org Biomol Chem] 2013 May 14; Vol. 11 (18), pp. 3046-56.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Royal+Society+of+Chemistry%22">Royal Society of Chemistry </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101154995 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1477-0539 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214770520%22">14770520 </searchLink><i>NLM ISO Abbreviation: </i>Org Biomol Chem <i>Subsets: </i>MEDLINE
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        Value: 10.1039/c3ob40407b
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      – Code: eng
        Text: English
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        StartPage: 3046
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              Text: 2013 May 14
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