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ScientificWorldJournal ; 11: 1489-95, 2011 Jul 28.
Article in English | MEDLINE | ID: mdl-21805018

ABSTRACT

Fifteen 7-chloro-4-arylhydrazonequinolines have been evaluated for their in vitro antifungal activity against eight oral fungi: Candida albicans, C. parapsilosis, C. lipolytica, C. tropicalis, C. famata, C. glabrata, Rhodutorula mucilaginosa, and R. glutinis. Several compounds exhibited minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) activities comparable with the first-line drug fluconazole. These results could be considered as an important starting point for the rational design of new antifungal agents.


Subject(s)
Antifungal Agents/pharmacology , Candida/drug effects , Hydrazones/pharmacology , Quinolines/pharmacology , Antifungal Agents/chemical synthesis , Antifungal Agents/chemistry , Candida albicans/drug effects , Hydrazones/chemical synthesis , Hydrazones/chemistry , Microbial Sensitivity Tests , Quinolines/chemical synthesis , Quinolines/chemistry
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