Glucosyl-1,2,3-triazoles derived from eugenol and analogues : synthesis, anti-Candida activity, and molecular modeling studies in CYP-51.

Registro completo de metadados
MetadadosDescriçãoIdioma
Autor(es): dc.creatorMagalhães, Lorena Severiano de-
Autor(es): dc.creatorReis, Adriana Cotta Cardoso-
Autor(es): dc.creatorNakao, Izadora Amaral-
Autor(es): dc.creatorPéret, Vinícius Augusto Campos-
Autor(es): dc.creatorReis, Rúbia Castro Fernandes Melo-
Autor(es): dc.creatorSilva, Naiara Chaves-
Autor(es): dc.creatorDias, Amanda Latercia Tranches-
Autor(es): dc.creatorCarvalho, Diogo Teixeira-
Autor(es): dc.creatorDias, Danielle Ferreira-
Autor(es): dc.creatorBrandão, Geraldo Célio-
Autor(es): dc.creatorBraga, Saulo Fehelberg Pinto-
Autor(es): dc.creatorSouza, Thiago Belarmino de-
Data de aceite: dc.date.accessioned2025-08-21T15:33:11Z-
Data de disponibilização: dc.date.available2025-08-21T15:33:11Z-
Data de envio: dc.date.issued2022-12-06-
Data de envio: dc.date.issued2022-12-06-
Data de envio: dc.date.issued2020-
Fonte completa do material: dc.identifierhttp://www.repositorio.ufop.br/jspui/handle/123456789/15873-
Fonte completa do material: dc.identifierhttps://onlinelibrary.wiley.com/doi/full/10.1111/cbdd.13948-
Fonte completa do material: dc.identifierhttps://doi.org/10.1111/cbdd.13948-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/1018135-
Descrição: dc.descriptionThis work describes the synthesis, anti-Candida, and molecular modeling stud- ies of eighteen new glucosyl-1,2,3-triazoles derived from eugenol and corre- lated phenols. The new compounds were characterized by combined Fourier Transform Infrared, 1 H and 13C nuclear magnetic resonance and spectroscopy of high-resolution mass spectrometry. The synthesized compounds did not show significant cytotoxicity against healthy fibroblast human cells (MCR-5) providing interesting selectivity indexes (SI) to active compounds. Considering the antifun- gal activity, nine compounds showed anti-Candida potential and the peracety- lated triazoles 17 and 18 were the most promising ones. Eugenol derivative 17 was active against three species of Candida at 26.1–52.1 μM. This compound was four times more potent than fluconazole against Candida krusei and less toxic (SI > 6.6) against the MCR-5 cells than fluconazole (SI > 3.3) considering this strain. Dihydroeugenol derivative 18 showed similar activity to 17 and was four times more potent and less toxic than fluconazole against C. krusei. The deacety- lated glucosides and non-glucosylated corresponding derivatives did not show considerable antifungal action, suggesting that the acetyl groups are essential for their anti-Candida activity. Molecular docking coupled with molecular dynam- ics showed that 14α-lanosterol demethylase is a feasible molecular target, since 17 and 18 could bind to this enzyme once deacetylated in vivo, thereby acting as prodrugs. Also, these studies demonstrated the importance of hydrophobic sub- stituents at the phenyl ring.-
Formato: dc.formatapplication/pdf-
Idioma: dc.languageen-
Direitos: dc.rightsrestrito-
Palavras-chave: dc.subjectMolecular docking-
Palavras-chave: dc.subjectMolecular dynamics-
Título: dc.titleGlucosyl-1,2,3-triazoles derived from eugenol and analogues : synthesis, anti-Candida activity, and molecular modeling studies in CYP-51.-
Aparece nas coleções:Repositório Institucional - UFOP

Não existem arquivos associados a este item.