Layton Tovar, Cristian FCuevas Yañez, ErickVelasco Montejo, Bayardo EMendieta Zerón, Hugo2026-03-232026-03-232014http://www.scielo.org.bo/scielo.php?script=sci_arttext&pid=S0250-54602014000100004&tlng=enhttps://andeanlibrary.org/handle/123456789/90164Vol. 31, No. 1Tetrahydrofuranosyl-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.Tetrahydrofuranosyl-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.enantimycotic effectClick ChemistrytriazolesArtículo Científico Publicado