dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorBruni, A. T.
dc.creatorLeite, VBP
dc.creatorFerreira, MMC
dc.date2014-05-20T15:22:20Z
dc.date2016-10-25T17:56:00Z
dc.date2014-05-20T15:22:20Z
dc.date2016-10-25T17:56:00Z
dc.date2002-01-30
dc.date.accessioned2017-04-05T23:36:06Z
dc.date.available2017-04-05T23:36:06Z
dc.identifierJournal of Computational Chemistry. Malden: Wiley-blackwell, v. 23, n. 2, p. 222-236, 2002.
dc.identifier0192-8651
dc.identifierhttp://hdl.handle.net/11449/33333
dc.identifierhttp://acervodigital.unesp.br/handle/11449/33333
dc.identifier10.1002/jcc.10004
dc.identifierWOS:000173053400003
dc.identifierhttp://dx.doi.org/10.1002/jcc.10004
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/877466
dc.descriptionIn conformational analysis, the systematic search method completely maps the space but suffers from the combinatorial explosion problem because the number of conformations increases exponentially with the number of free rotation angles. This study introduces a new methodology of conformational analysis that controls the combinatorial explosion. It is based on a dimensional reduction of the system through the use of principal component analysis. The results are exactly the same as those obtained for the complete search but, in this case, the number of conformations increases only quadratically with the number of free rotation angles. The method is applied to a series of three drugs: omeprazole. pantoprazole, lansoprazole-benzimidazoles that suppress gastric-acid secretion by means of H(+), K(+)-ATPase enzyme inhibition. (C) 2002 John Wiley Sons. Inc.
dc.languageeng
dc.publisherWiley-Blackwell
dc.relationJournal of Computational Chemistry
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectprincipal component analysis
dc.subjectchemometrics
dc.subjectomeprazole
dc.subjectpantoprazole
dc.subjectlansoprazole
dc.subjectconformational analysis
dc.titleConformational analysis: A new approach by means of chemometrics
dc.typeOtro


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