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dc.contributor.authorArango Acosta, Gabriel Jaime-
dc.contributor.authorJaramillo Flórez, María Consuelo-
dc.contributor.authorMora Arango, Cristina Lucía-
dc.contributor.authorVélez, Luis Esteban-
dc.contributor.authorQuijano Tobón, Jairo-
dc.date.accessioned2024-02-18T15:25:43Z-
dc.date.available2024-02-18T15:25:43Z-
dc.date.issued2006-
dc.identifier.issn1827-8620-
dc.identifier.urihttps://hdl.handle.net/10495/38198-
dc.description.abstractABSTRACT: The appearance of bacterial resitance due to β-lactamase enzyme is frequent in Colombia and it has important consequences in term of morbidity and mortality. The inhibitory evaluation of the β-lactamase enzyme of 5 compounds gave as a result more powerful compounds than clavulanic acid. The more active chalcones establish hydrogen bonds with Ser, Tyr and Lys amino acids, the high number of hydrogen bonds between the compound and the amino acid increases the affinity and the inhibitory activity. In accordance with the results, the compounds might inhibit irreversibly the β-lactamase enzyme.spa
dc.format.extent6 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherUniversity of Salernospa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/*
dc.titleBiological evaluation of aromatic compounds as B-Lactamase inhibitorsspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGrupo de Investigación en Sustancias Bioactivas (GISB)spa
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
oaire.citationtitlePharmacologyonlinespa
oaire.citationstartpage650spa
oaire.citationendpage655spa
oaire.citationvolume3spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-nd/4.0/spa
dc.publisher.placeSalerno, Italiaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsbeta-Lactamasas-
dc.subject.decsbeta-Lactamases-
dc.subject.decsÁcido Clavulánico-
dc.subject.decsClavulanic Acid-
dc.subject.decsInhibidores Enzimáticos-
dc.subject.decsEnzyme Inhibitors-
dc.subject.decsAmoxicilina-
dc.subject.decsAmoxicillin-
dc.subject.decsChalcona-
dc.subject.decsChalcone-
dc.description.researchgroupidCOL0010359spa
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D001618-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D019818-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D004791-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D000658-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D002599-
dc.relation.ispartofjournalabbrevPharmacologyonlinespa
Aparece en las colecciones: Artículos de Revista en Farmacéutica y Alimentarias

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