2,3-Dihydro-5-benzofuranols as antioxidant-based inhibitors of leukotriene biosynthesis
- 1 May 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 32 (5) , 1006-1020
- https://doi.org/10.1021/jm00125a014
Abstract
Note: In lieu of an abstract, this is the article's first page.This publication has 15 references indexed in Scilit:
- Structural requirements for the inhibition of 5-lipoxygenase by 15-hydroxyeicosa-5,8,11,13-tetraenoic acid analogsJournal of Medicinal Chemistry, 1987
- Substituted arylmethyl phenyl ethers. 1. A novel series of 5-lipoxygenase inhibitors and leukotriene antagonistsJournal of Medicinal Chemistry, 1987
- Kinetic mechanism of guinea pig neutrophil 5-lipoxygenase.Journal of Biological Chemistry, 1986
- Autoxidation of biological molecules. 4. Maximizing the antioxidant activity of phenolsJournal of the American Chemical Society, 1985
- CAFFEIC ACID IS A SELECTIVE INHIBITOR FOR LEUKOTRIENE BIOSYNTHESIS1984
- Synthesis and 5-lipoxygenase inhibitory activities of eicosanoid compoundsJournal of Medicinal Chemistry, 1983
- Inhibition of leukotriene biosynthesis by acetylenic analogsBiochemical and Biophysical Research Communications, 1982
- In vitro effects of synthetic antioxidants and vitamin E on arachidonic acid metabolism and thromboxane formation in human platelets and on platelet aggregationProstaglandins, 1981
- Factors affecting the initial rate of lipoxygenase catalysisBiochemical and Biophysical Research Communications, 1981
- Leukotrienes are potent constrictors of human bronchiNature, 1980