Studies on Anti-inflammatory Agents. XLVI : Studies on the Synthesis and Analgesic-Anti-inflammatory Activities of Phenylacetic Acid Derivatives bearing Heteroaromatic Rings
Open Access
- 1 January 1977
- journal article
- research article
- Published by Pharmaceutical Society of Japan in YAKUGAKU ZASSHI
- Vol. 97 (8) , 835-848
- https://doi.org/10.1248/yakushi1947.97.8_835
Abstract
A series of phenylacetic acid and phenethyl alcohol derivatives with a bicyclic heteroaromatic ring were synthesized. Bicyclic heteroaromatic rings were imidazo[1,2-a]-pyridine, imidazo[2,1-b]thiazole, imidazo[1,2-a]pyrimidine and indolizine. These compounds were tested for analgesic and anti-inflammatory activity in the phenylquinone writhing [mouse] and carrageenin paw edema [rat] assays, and the relationship between their structure and activity was discussed. 2-[4-(Imidazo[1,2-a]-pyridin-2-yl)phenyl]propionic acid had the most potent activity.Keywords
This publication has 3 references indexed in Scilit:
- Derivatives of Imidazole. I. Synthesis and Reactions of Imidazo[1,2-α]pyridines with Analgesic, Antiinflammatory, Antipyretic, and Anticonvulsant ActivityJournal of Medicinal Chemistry, 1965
- Carrageenin-Induced Edema in Hind Paw of the Rat as an Assay for Antiinflammatory DrugsExperimental Biology and Medicine, 1962
- ANTAGONISM OF THE FREQUENCY OF PHENYLQUINONE-INDUCED WRITHING IN THE MOUSE BY WEAK ANALGESICS AND NONANALGESICS1959