Some 1-arylmethylimidazoles bearing a naphthyl group at the α position of benzyl moiety have been synthesized and tested as antifungal agents against Candida albicans and Candida spp. Such derivatives resemble bifonazole and naftifine, two important antimycotic agents of clinical use. Various compounds were found highly active when tested against Candida strains in comparison with bifonazole, miconazole, clotrimazole and ketoconazole.

Research on antibacterial and antifungal agents. 16. Synthesis and antifungal activities of 1-[α-(1-naphthyl)benzyl]imidazole derivatives and related 2-naphthyl isomers / Artico, Marino; Stefancich, Giorgio; Silvestri, Romano; Massa, Silvio; G., Apuzzo; Artico, Marco; G., Simonetti. - In: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY. - ISSN 0223-5234. - 27:(1992), pp. 693-699. [10.1016/0223-5234(92)90089-J]

Research on antibacterial and antifungal agents. 16. Synthesis and antifungal activities of 1-[α-(1-naphthyl)benzyl]imidazole derivatives and related 2-naphthyl isomers

ARTICO, Marino;SILVESTRI, Romano;ARTICO, Marco;
1992

Abstract

Some 1-arylmethylimidazoles bearing a naphthyl group at the α position of benzyl moiety have been synthesized and tested as antifungal agents against Candida albicans and Candida spp. Such derivatives resemble bifonazole and naftifine, two important antimycotic agents of clinical use. Various compounds were found highly active when tested against Candida strains in comparison with bifonazole, miconazole, clotrimazole and ketoconazole.
1992
01 Pubblicazione su rivista::01a Articolo in rivista
Research on antibacterial and antifungal agents. 16. Synthesis and antifungal activities of 1-[α-(1-naphthyl)benzyl]imidazole derivatives and related 2-naphthyl isomers / Artico, Marino; Stefancich, Giorgio; Silvestri, Romano; Massa, Silvio; G., Apuzzo; Artico, Marco; G., Simonetti. - In: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY. - ISSN 0223-5234. - 27:(1992), pp. 693-699. [10.1016/0223-5234(92)90089-J]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/470215
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