Structures and histamine release inhibitory effects of prenylated orcinol derivatives from Rhododendron dauricum

被引:109
作者
Iwata, N
Wang, NL
Yao, XS
Kitanaka, S
机构
[1] Nihon Univ, Coll Pharm, Funabashi, Chiba 2748555, Japan
[2] Shenyang Pharmaceut Univ, Shenyang 110015, Peoples R China
来源
JOURNAL OF NATURAL PRODUCTS | 2004年 / 67卷 / 07期
关键词
D O I
10.1021/np0303916
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Four new prenylated orcinol derivatives, daurichromenes A-D (1-4), along with three known compounds, confluentin (5), grifolin (6), and orcinol (7), have been isolated from the Chinese medicinal plant Rhododendron dauricum. Their structures were established as 2,R-(7'-hydroxy-4',8'-dimethyl-3'E,8'-nonadienyl)-5-hydroxy-2,7-dimethyl-2H-chromene (1), 2R-(3'-hydroxy-8'-methyl-4'-methyliden-7'-nonaenyl)-5-hydroxy-2,7-dimethyl-2H-chromene (2), 2R-(8'-hydroxy-4',8'-dimethyl-3'E,6'Z-nonadienyl)-5-hydroxy-2,7-dimethyl-2H-chromene (3), and 2R-(9'-hydroxy-4',8'-dimethyl-3'E,7'E-nonadienyl)-5-hydroxy-2,7-dimethyl-2H-chromene (4) by analysis of spectral data. The absolute configuration of the asymmetric carbons at the chromene ring in 1-5 was determined as R from their circular dichroism spectra. Compounds 1-6 significantly inhibited compound 48/80-induced histamine release from rat peritoneal mast cells.
引用
收藏
页码:1106 / 1109
页数:4
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