PISCICIDAL STEROL ACYLGLUCOSIDES FROM EDGEWORTHIA-CHRYSANTHA

被引：23

作者：

HASHIMOTO, T

TORI, M

ASAKAWA, Y

机构：

[1] Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Tokushima, 770, Yamashiro-cho

来源：

PHYTOCHEMISTRY | 1991年 / 30卷 / 09期

关键词：

EDGEWORTHIA-CHRYSANTHA; THYMELAEACEAE; FLOWER; SITOSTEROL-3-O-6-LINOLEOYL- AND SITOSTEROL-3-O-6-LINOLENOYL-BETA-D-; GLUCOPYRANOSIDES; GRASSHOPPER KETONE; DAPHNORETIN; PISCICIDAL ACTIVITY; SYNTHESIS OF CHRYSANTHOSIDE;

D O I：

10.1016/S0031-9422(00)98226-8

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

New potent piscicidal sterol acylglucosides named chrysanthosides have been obtained from the flower of Edgeworthia chrysantha, together with the previously known bis-coumarin and grasshopper ketone and their structures characterized to be sitosterol-3-O-6-linoleoyl- and sitosterol-3-O-6-linolenoyl-beta-D-glucopyranosides by spectral data and synthesis. The natural and synthetic chrysanthosides possess potent piscicidal activity against killie-fish which was killed within 3 hr at a concentration of 0.1 ppm.

引用

页码：2927 / 2931

页数：5

共 17 条

[1]

ASAKAWA Y, 1990, CHEM CHEM TAXONOMY B, P369

[2]

CHAKRABARTI R, 1986, PHYTOCHEMISTRY, V25, P558

[3]

GHOSAL S, 1984, J CHEM RES-S, P110

[4] A HIGHLY EFFICIENT PREPARATION OF LUNULARIC ACID AND SOME BIOLOGICAL-ACTIVITIES OF STILBENE AND DIHYDROSTILBENE DERIVATIVES [J].