Etya

Etya is a lipid of Fatty Acyls (FA) class.

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There are no associated biomedical information in the current reference collection.

Current reference collection contains 2345 references associated with Etya in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

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Authors Title Published Journal PubMed Link
McCluskey ER et al. Temporal changes in 12-HETE formation in two models of canine myocardial infarction. 1985 Prostaglandins pmid:3923561
Hidaka T et al. Metabolism of [14C] arachidonic acid in the isolated rabbit spleen. 1980 Prostaglandins pmid:7422893
Taylor AS et al. Incorporation of 5,8,11,14-eicosatetraynoic acid (ETYA) into cell lipids: competition with arachidonic acid for esterification. 1985 Prostaglandins pmid:3923563
Levy JV Changes in systolic arterial blood pressure in normal and spontaneously hypertensive rats produced by acute administration of inhibitors of prostaglandin biosynthesis. 1977 Prostaglandins pmid:841102
Channing CP Effects of prostaglandin inhibitors, 7-oxa-13-prostynoic acid and eicosa-5,8,11,14-tetraynoic acid, upon luteinization of rhesus monkey granulosa cells in culture. 1972 Prostaglandins pmid:4631748
Yamamoto A et al. Arachidonate lipoxygenase inhibitors in guinea-pig isolated trachea. Effects on contractions to antigen and various agonists. 1990 Prostaglandins pmid:1965555
Newton RC The production of human interleukin-1 beta by blood monocytes. 1990 Prog. Clin. Biol. Res. pmid:2204930
Sparrow CP and Olszewski J Cellular oxidative modification of low density lipoprotein does not require lipoxygenases. 1992 Proc. Natl. Acad. Sci. U.S.A. pmid:1729678
Marin P et al. Somatostatin potentiates the alpha 1-adrenergic activation of phospholipase C in striatal astrocytes through a mechanism involving arachidonic acid and glutamate. 1991 Proc. Natl. Acad. Sci. U.S.A. pmid:1681548
Kalgutkar AS et al. Biochemically based design of cyclooxygenase-2 (COX-2) inhibitors: facile conversion of nonsteroidal antiinflammatory drugs to potent and highly selective COX-2 inhibitors. 2000 Proc. Natl. Acad. Sci. U.S.A. pmid:10639181