Inhibition of leukotriene biosynthesis by acetylenic analogs
- 1 July 1982
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 107 (1), 101-108
- https://doi.org/10.1016/0006-291x(82)91675-8
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Enzymatic formation of 14,15-leukotriene A and C(14)-sulfur-linked peptidesBiochemical and Biophysical Research Communications, 1982
- Transformation of 15‐hydroperoxy‐5,9,11,13‐eicosatetraenoic acid into novel leukotrienesFEBS Letters, 1981
- Novel leukotrienes: Products formed by initial oxygenation of arachidonic acid at C-15Biochemical and Biophysical Research Communications, 1981
- Leukotriene A4: Enzymatic conversion to leukotriene C4Biochemical and Biophysical Research Communications, 1980
- Calcium stimulation of a novel lipoxygenaseBiochemical and Biophysical Research Communications, 1980
- Synthesis of [5,6-3H]arachidonic acid and its use in development of a sensitive assay for prostacyclin synthetaseBiochemistry, 1980
- Generation of unique mono-hydroxy-eicosatetraenoic acids from arachidonic acid by human neutrophils.The Journal of Experimental Medicine, 1979
- Synthesis from arachidonic acid of potential prostaglandin precursorsJournal of the Chemical Society, Perkin Transactions 1, 1979
- Inhibition of prostaglandin biosynthesis by eicosa-5,8,11,14-tetraynoic acidBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1970
- Enzyme inhibition by acetylenic compoundsBiochemical and Biophysical Research Communications, 1970