Abstract
Among the different xanthones previously isolated from the stem bark of Calophyllum caledonicum , caledonixanthone E presented the strongest activity (MIC80 = 8 μg/mL) in acidic conditions (pH 3) against the human pathogenic fungus Aspergillus fumigatus . Phase-contrast microscopy studies suggested the assembly or synthesis of cell wall components as the target of the drug. Moreover, the use of fluorescent lectins further supported an impact of caledonixanthone E on the synthesis of chitin, the major structural polysaccharide of the fungal wall. These results suggest that caledonixanthone E may be an interesting model for the design of new antifungal drugs.
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Dr. Gérald Larcher
GEIHP
UPRES-EA 3142
Laboratoire de Parasitologie-Mycologie
Centre Hospitalier Universitaire
4 rue Larrey
49033 Angers
France
Phone: +33-02-41-35-34-72
Fax: +33-02-41-35-36-16
Email: gerald.larcher@univ-angers.fr