dc.creatorBraga, S F
dc.creatorGalvão, D S
dc.date2002-Aug
dc.date2015-11-27T12:49:21Z
dc.date2015-11-27T12:49:21Z
dc.date.accessioned2018-03-29T00:56:40Z
dc.date.available2018-03-29T00:56:40Z
dc.identifierJournal Of Molecular Graphics & Modelling. v. 21, n. 1, p. 57-70, 2002-Aug.
dc.identifier1093-3263
dc.identifier
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/12413032
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/195182
dc.identifier12413032
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1295415
dc.descriptionWe performed a conformational and electronic analysis for 10-deacetylbaccatin-III (DBAC) using well-known semiempirical methods (parametric method 3 (PM3) and Zerner's intermediate neglect of differential overlap (ZINDO)) coupled to the concepts of total and local density of states (LDOS). Our results indicate that regions presented by paclitaxel (Taxol) as important for the biological activity can be traced out by the electronic features present in DBAC. These molecules differ only by a phenylisoserine side chain. Compared to paclitaxel, DBAC has a simpler structure in terms of molecular size and number of degrees of freedom (d.f.). This makes DBAC a good candidate for a preliminary investigation of the taxoid family. Our results question the importance of the oxetane group, which seems to be consistent with recent experimental data.
dc.description21
dc.description57-70
dc.languageeng
dc.relationJournal Of Molecular Graphics & Modelling
dc.relationJ. Mol. Graph. Model.
dc.rightsfechado
dc.rights
dc.sourcePubMed
dc.subjectAlkaloids
dc.subjectDrugs, Chinese Herbal
dc.subjectElectrochemistry
dc.subjectHumans
dc.subjectModels, Chemical
dc.subjectMolecular Conformation
dc.subjectMolecular Structure
dc.subjectPaclitaxel
dc.subjectTaxoids
dc.titleA Semiempirical Study On The Electronic Structure Of 10-deacetylbaccatin-iii.
dc.typeArtículos de revistas


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