Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Stereospecific Inversion of Configuration of 2-(2-Isopropylindan-5-yl)-propionic Acid in Rats
YORIHISA TANAKARYOZO HAYASHI
Author information
Keywords: NMR
JOURNAL FREE ACCESS

1980 Volume 28 Issue 8 Pages 2542-2545

Details
Abstract
The d-tertiary hydroxy metabolite, which was isolated from rat urine after oral administration of 3, 3, 3-d3-l-2-(2-isopropylindan-5-yl) propionic acid (IIPA), was confirmed to retain the intact CD3 group on the basis of the MS and NMR spectral analyses. This finding is not compatible with the exomethylene intermediate mechanism proposed for the same epimerization reaction of 2-(4-isobutylphenyl) propionic acid (ibuprofen) in human.
Content from these authors
© The Pharmaceutical Society of Japan
Previous article Next article
feedback
Top