Glycerides as prodrugs. 1. Synthesis and antiinflammatory activity of 1,3-bis(alkanoyl)-2-(O-acetylsalicyloyl)glycerides (aspirin triglycerides)
- 1 June 1979
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 22 (6) , 683-687
- https://doi.org/10.1021/jm00192a014
Abstract
A series of 1,3-bis(alkanoyl)-2-(O-acetylsalicyloyl)glycerides (aspirin triglycerides) having aspirin at the 2 position of glycerol and fatty acids at the 1 and 3 positions was prepared. The compounds were administered orally and tested for efficacy in the rat paw edema test and the stomachs were examined for the presence of lesions. The members of this series in which the fatty acids are of intermediate chain length (C4-C12) do not cause gastric lesions and have essentially all the systemic activity associated with aspirin.This publication has 4 references indexed in Scilit:
- A Comparison of a New Slow Release Aspirin (“Slow Aspirin”) with Plain Aspirin in the Treatment of Rheumatoid DiseaseJournal of International Medical Research, 1977
- Glyceride isomerizations in lipid chemistryJournal of Oil & Fat Industries, 1967
- Carrageenin-Induced Edema in Hind Paw of the Rat as an Assay for Antiinflammatory DrugsExperimental Biology and Medicine, 1962
- A Study of the Factors Involved in the Production of Gastric Ulcers by the Restraint TechniqueGastroenterology, 1960