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Chemical Studies on the Orient Plant Drugs‐II Structure of Glycoside‐P 1 , A Steryl Glucoside of Panax Ginseng Rhizoma
Author(s) -
Lin TzongDann,
Lin MeiChao
Publication year - 1976
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.197600016
Subject(s) - chemistry , ginseng , araliaceae , glucoside , glycoside , hydrolysis , ginsenoside , saponin , derivative (finance) , chemical structure , acid hydrolysis , stereochemistry , organic chemistry , medicine , alternative medicine , pathology , financial economics , economics
A new component of the steryl glucoside of Panax ginseng C.A. Meyer (Araliaceae) has been identified as sitosteryl–β–D–(6–O–fattyacyl)–glucopyranoside (1). Its gross structure, as a monoester of β–sitosteryl, campesteryl and stigmasteryl–β–D‐glucoside, was derived from a study of the products formed on methanolysis and on acid hydrolysis. The location of the fatty ester was established by comparison of the proton chemical shift for H 2 C–6 in its tribenzoyl derivative with the chemical shifts for the corresponding protons in model benzoyl and acetyl derivation of sitosteryl–β–D–glucopyranoside.

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