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dc.creatorGuevara-Salazar, Alberto-
dc.creatorQuintana-Zavala, Delia-
dc.creatorEspinoza-Fonseca, Michel-
dc.creatorCorrea-Basurto, Jose-
dc.creatorTrijillo-Ferrara, Jose-
dc.date2012-03-29T21:25:08Z-
dc.date2012-03-29T21:25:08Z-
dc.date2007-10-01-
dc.date.accessioned2013-01-16T16:41:59Z-
dc.date.available2013-01-16T16:41:59Z-
dc.date.issued2013-01-16-
dc.identifier1665-9686-
dc.identifierhttp://hdl.handle.net/123456789/1225-
dc.identifier.urihttp://www.repositoriodigital.ipn.mx/handle/123456789/11692-
dc.descriptionA computational docking approach, in combination with the Hammett relationship, has been employed to evaluate the electronic influence of substituents on ligand binding and the active site-directed inhibitory potency on acetylcholinesterase using nine N-aryl-substituted succinimides. Our results indicate that electronwithdrawing groups attached to benzene moiety of the compounds favor the inhibitory potency while electron-donating groups do not. This fact was confirmed by performing kinetic experiments on acetylcholinesterase from Electrophorus electricus; the experiments showed that para-substituted-NO2 compound inhibits better than para-substituted-OMe and –H derivatives. This approach may be useful for the rationalization of drugs design, as well as the mechanism of the active site.-
dc.descriptionInstituto Politecnico Nacional, CONACYT-
dc.languageen-
dc.publisherJournal of the Mexican Chemical Society-
dc.relation;51, 222-227-
dc.subjectAcetylcholinesterase-
dc.subjectHammett Relationship-
dc.subjectDocking,-
dc.subjectN-aryl-substituted-succinimides-
dc.titleThe Electronic Influence on the Active Site-Directed Inhibition of-
dc.typeArticle-
Aparece en las colecciones: Doctorado

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