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1.
Nat Prod Res ; 25(12): 1185-9, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21740284

ABSTRACT

The methanolic crude extract from the roots of Jacquinia flammea showed moderate antifungal activity against dermatophytes and very strong antifungal activity against Colletotrichum gloeosporioides. The bioassay-guided purification of the extract, using a combination of vacuum-liquid chromatography and high performance liquid chromatography, allowed the identification of sakurasosaponin as the main metabolite responsible for the antifungal activity.


Subject(s)
Antifungal Agents/pharmacology , Plant Extracts/pharmacology , Plant Roots/chemistry , Primulaceae/chemistry , Saponins/pharmacology , Antifungal Agents/analysis , Antifungal Agents/chemistry , Arthrodermataceae/drug effects , Chromatography, Liquid , Colletotrichum/drug effects , Methanol , Molecular Structure , Plant Extracts/analysis , Plant Extracts/chemistry , Saponins/analysis , Saponins/chemistry
2.
Bioorg Med Chem ; 16(17): 7908-20, 2008 Sep 01.
Article in English | MEDLINE | ID: mdl-18752959

ABSTRACT

Diverse polyfunctionalized quinolines, easily prepared using Lewis acid-catalyzed imino Diels-Alder reactions between corresponding aldimines, were tested for antifungal properties against standardized as well as clinical isolates of clinically important fungi. Among them, 4-pyridyl derivatives displayed the best activities mainly against dermatophytes. The activity appears not to be related neither to the lipophilicity nor to the basicity of compounds.


Subject(s)
Antifungal Agents/chemical synthesis , Antifungal Agents/pharmacology , Candida/drug effects , Cryptococcus/drug effects , Quinolines/chemical synthesis , Quinolines/pharmacology , Acids/chemistry , Antifungal Agents/chemistry , Arthrodermataceae/drug effects , Arthrodermataceae/growth & development , Candida/growth & development , Catalysis , Cryptococcus/growth & development , Dose-Response Relationship, Drug , Imines/chemistry , Microbial Sensitivity Tests , Molecular Structure , Quinolines/chemistry , Stereoisomerism , Structure-Activity Relationship
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