Six new dibenzofuran glycosides, fortuneanosides G (1), H (2), I (3), J (4), K (5), and L (6), were isolated from the fruit of Pyracantha fortuneana (MAXIM) LI. Their structures were determined to be 3,7-dihydroxy-2,4-dimethoxy- dibenzofuran 7-O-β-D-glucopyranoside, 3,7-dihydroxy-2,4-dimethoxy- dibenzofuran 7-O-(α-L-rhamnopyranosyl)-(1-6)-β-D-glucopyranoside, 3,6-dihydroxy-2,4-dimethoxy-dibenzofuran 6-O-β-D-glucopyranoside, 2,4-dimethoxy-3,6,9-trihydroxy-dibenzofuran 6-O-β-D-glucopyranoside, 3,9-dihydroxy-2,4-dimethoxydibenzofuran 3-O-β-D-glucopyranoside, and 2-methoxy-3,4,9-trihydroxy-dibenzofuran 4-O-β-D-glucopyranoside based on spectroscopic analysis. Fortuneanosides G-J showed more potent tyrosinase-inhibitory activity than arbutin. © 2008 Pharmaceutical Society of Japan.
CITATION STYLE
Dai, Y., Zhou, G. X., Kurihara, H., Ye, W. C., & Yao, X. S. (2008). Fortuneanosides G-L, dibenzofuran glycosides from the fruit of pyracantha fortuneana. Chemical and Pharmaceutical Bulletin, 56(4), 439–442. https://doi.org/10.1248/cpb.56.439
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