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Please use this identifier to cite or link to this item: http://ri.uaemex.mx/handle20.500.11799/40375
DC FieldValueLanguage
dc.creatorCRISTIAN FABIAN LAYTON TOVAR-
dc.creatorErick Cuevas Yáñez-
dc.creatorBAYARDO ESAU VELASCO MONTEJO-
dc.creatorHugo Mendieta Zerón-
dc.date2014-
dc.identifierhttp://hdl.handle.net/20.500.11799/40375-
dc.descriptionTetrahydrofuranosyl-1,2,3-triazoles, synthesized by Click chemistry, were tested as novel antifungal compounds. The results show a remarkable activity against Candida albicans ATCC 10231 expressed in a high MIC50 and MIC90 compared to traditional antifungals such as fluconazole.-
dc.formatapplication/application/pdf-
dc.languageeng-
dc.publisherUniversidad Mayor de San Andrés-
dc.relationhttp://www.redalyc.org/revista.oa?id=4263-
dc.rightsinfo:eu-repo/semantics/Revista Boliviana de Química-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/4.0-
dc.sourceRevista Boliviana de Química (Bolivia) Num.1 Vol.31-
dc.subjectQuímica-
dc.subjectAntimycotic effect-
dc.subjectClick Chemistry-
dc.subjecttriazoles-
dc.subjectinfo:eu-repo/classification/cti/2-
dc.titleHIGH SUSCEPTIBILITY OF CANDIDA ALBICANS ATCC 10231 TO TETRAHYDROFURANOSYL-1,2,3-TRIAZOLES OBTAINED BY CLICK CHEMISTRY-
dc.titleHigh susceptibility of candida albicans atcc 10231 to tetrahydrofuranosyl-1,2,3-triazoles obtained by click chemistry-
dc.typearticle-
dc.audiencestudents-
dc.audienceresearchers-
item.grantfulltextnone-
item.fulltextNo Fulltext-
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