Syntheses of Estriol Monoglucuronides.
- 1 January 1967
- journal article
- research article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 15 (8) , 1232-1238
- https://doi.org/10.1248/cpb.15.1232
Abstract
Syntheses of estriol glucosiduronic acids were carried out employing Koenings-Knorr reaction. Of these three 16- and 17-glucuronides were prepared from estrone 3-benzyl ether, and 3-isomer from estriol 16,17-diacetate. All the glucuronides thus obtained underwent hydrolysis with beef liver [beta] -glucuronidase to furnish estriol and glucuronic acid.This publication has 3 references indexed in Scilit:
- Use of sephadex ion exchanger for the separation of conjugated urinary estrogensAnalytical Biochemistry, 1965
- OESTRIOL METABOLISM IN PREGNANT WOMENActa Endocrinologica, 1964
- Isolation and Characterization of Estriol 16α-Glucosiduronic Acid from Human Pregnancy UrineJournal of Biological Chemistry, 1963