The use of radioisotopically labelled methyl esters in the determination of the 15-epimer content of prostaglandins
- 1 November 1973
- journal article
- Published by Oxford University Press (OUP) in Journal of Pharmacy and Pharmacology
- Vol. 25 (11) , 900-904
- https://doi.org/10.1111/j.2042-7158.1973.tb09970.x
Abstract
The quantitative determination of the 15-epimer content of prostaglandins by formation of their isotopically-labelled methyl esters is described. Either [3H]dimethyl sulphate or [14C]diazomethane are used as esterification reagents. The reaction products are separated by thin layer chromatography and the epimer ratio determined by scintillation counting of the labelled ester zones. The accuracy of the technique is illustrated by the determination of 15-epimer in ICI 74 205, a close analogue of PGF2α. Evidence for the uncatalysed reaction of diazomethane with the alcoholic hydroxyl groups of prostaglandin molecules, which could be significant in other prostaglandin analysis techniques (e.g. g.l.c.) which depend on quantitative esterification with this reagent, is also presented.Keywords
This publication has 6 references indexed in Scilit:
- Quantitative determination of 15-epi-PGF2α in PGF2αProstaglandins, 1972
- New reagents for stereoselective carbonyl reduction. Improved synthetic route to the primary prostaglandinsJournal of the American Chemical Society, 1971
- Base-Catalyzed Preparation of Methyl and Ethyl Esters of Carboxylic AcidsThe Journal of Organic Chemistry, 1964
- Esterification of Fatty Acids with Diazomethane on a Small ScaleAnalytical Chemistry, 1960
- Die Methylierung von Trioxy‐glutarsäuren und Weinsäure mit Diazo‐methanBerichte der deutschen chemischen Gesellschaft (A and B Series), 1934
- Untersuchungen über Eigenschaftsänderungen chemischer Verbindungen durch Komplexbildung. VI. Über die Methylierung von Alkoholen mittels DiazomethanEuropean Journal of Organic Chemistry, 1930