Azide-enolate 1,3-dipolar cycloaddition in the synthesis of novel triazole-based miconazole analogues as promising antifungal agents.
Eur J Med Chem
; 112: 60-65, 2016 Apr 13.
Article
em En
| MEDLINE
| ID: mdl-26890112
ABSTRACT
Seven miconazole analogs involving 1,4,5-tri and 1,5-disubstituted triazole moieties were synthesized by azide-enolate 1,3-dipolar cycloaddition. The antifungal activity of these compounds was evaluated in vitro against four filamentous fungi, including Aspergillus fumigatus, Trichosporon cutaneum, Rhizopus oryzae, and Mucor hiemalis as well as three species of Candida spp. as yeast specimens. These pre-clinical studies suggest that compounds 4b, 4d and 7b can be considered as drug candidates for future complementary biological studies due to their good/excellent antifungal activities.
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Texto completo:
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Base de dados:
MEDLINE
Assunto principal:
Triazóis
/
Fungos
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Miconazol
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Antifúngicos
Limite:
Humans
Idioma:
En
Ano de publicação:
2016
Tipo de documento:
Article