A new aurone glycoside with antifungal activity from marine-derived fungus Penicillium sp. FJ-1.
- Author:
Yan-xia SONG
;
Qiang MA
;
Jie LI
- Publication Type:Journal Article
- MeSH:
Antifungal Agents;
chemistry;
isolation & purification;
metabolism;
pharmacology;
Benzofurans;
chemistry;
isolation & purification;
metabolism;
pharmacology;
Candida;
drug effects;
Glycosides;
chemistry;
isolation & purification;
metabolism;
pharmacology;
Molecular Structure;
Penicillium;
chemistry;
genetics;
isolation & purification;
metabolism;
Seawater;
microbiology
- From:
China Journal of Chinese Materia Medica
2015;40(6):1097-1101
- CountryChina
- Language:English
-
Abstract:
Endophytic fungi which reside in the tissue of mangrove plants seem to play an important role in the discovery of new biologically active substances. During the course of screening for the antimicrobial metabolites from the endophytic fugus Penicillium sp. FJ-1 of mangrove plant Avicennia marina, a new aurone glycoside (1) was isolated by repeated column chromatography on silica gel and recrystallization methods. The structure of 1 was elucidated as (Z)-7,4'-dimethoxy-6-hydroxy-aurone-4-O-β-glucopyranoside, on the basis of spectroscopic analysis. Compound 1 exhibited antifungal activity against Candida sp., with the potency comparable to amphotericin B and much better than fluconazole. Compound 1 can also inhibit extracellular phospholipase secretion in a concentration-dependent manner.
