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Please use this identifier to cite or link to this item: http://ri.uaemex.mx/handle20.500.11799/104557
DC FieldValueLanguage
dc.creatorCRISTIAN FABIAN LAYTON TOVAR-
dc.creatorErick Cuevas Yáñez-
dc.creatorBAYARDO ESAU VELASCO MONTEJO-
dc.creatorHugo Mendieta Zerón-
dc.date2014-06-30-
dc.date.accessioned2022-04-21T06:01:42Z-
dc.date.available2022-04-21T06:01:42Z-
dc.identifierhttp://hdl.handle.net/20.500.11799/104557-
dc.identifier.urihttp://ri.uaemex.mx/handle20.500.11799/104557-
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.languageeng-
dc.publisherRevista Boliviana-
dc.relationVol.;31-
dc.relationNo.;1-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/4.0-
dc.source2078-3949-
dc.subjectSusceptibility-
dc.subjectCandida albicans ATCC 10231-
dc.subjectTETRAHIDROFURANOSIL-1, 2, 3-TRIAZOLES-
dc.subjectVia click-
dc.subjectSensititre yeast one-
dc.subjectYeast microdilution-
dc.subjectinfo:eu-repo/classification/cti/3-
dc.titleSusceptibility of Candida albicans ATCC 10231 to TETRAHIDROFURANOSIL-1, 2, 3-TRIAZOLES obtained by “Via click” with evaluation of the sensititre yeast one and yeast microdilution methods-
dc.typearticle-
dc.audiencestudents-
dc.audienceresearchers-
item.grantfulltextnone-
item.fulltextNo Fulltext-
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