Search Results - "Rokach, J"
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Biochemistry, biology and chemistry of the 5-lipoxygenase product 5-oxo-ETE
Published in Progress in lipid research (01-03-2005)“…5-Oxo-ETE (5-oxo-6,8,11,14-eicosatetraenoic acid) is an arachidonic acid metabolite formed by the oxidation of 5 S-hydroxy-6,8,11,14-eicosatetraenoic acid…”
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Biomarkers of oxidative stress study III. Effects of the nonsteroidal anti-inflammatory agents indomethacin and meclofenamic acid on measurements of oxidative products of lipids in CCl4 poisoning
Published in Free radical biology & medicine (15-03-2005)“…Plasma and urinary levels of malondialdehyde-like products (MDA) and isoprostanes were identified as markers of in vivo lipid peroxidation in an animal model…”
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Localization of distinct F2-isoprostanes in human atherosclerotic lesions
Published in The Journal of clinical investigation (15-10-1997)“…F2-Isoprostanes are prostaglandin (PG) isomers formed in situ in cell membranes by peroxidation of arachidonic acid. 8-epi PGF2alpha and IPF2alpha-I are…”
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The Isoprostanes: A Perspective
Published in Prostaglandins (01-12-1997)“…The isoprostanes are a new class of natural products produced in vivo by a non-enzymatic free-radical-induced peroxidation of polyunsaturated fatty acid. In…”
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Leukotrienes, lipoxins, and hydroxyeicosatetraenoic acids
Published in Methods in molecular biology (Clifton, N.J.) (1999)Get more information
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Pharmacology of L-660,711 (MK-571): a novel potent and selective leukotriene D4 receptor antagonist
Published in Canadian journal of physiology and pharmacology (01-01-1989)“…L-660,711 (3-(3-(2-(7-chloro-2-quinolinyl)ethenyl)phenyl) ((3-dimethyl amino-3-oxo propyl)thio)methyl)thio)propanoic acid is a potent and selective competitive…”
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L-663,536 (MK-886) (3-[1-(4-chlorobenzyl)-3-t-butyl-thio-5-isopropylindol-2-yl]-2,2 - dimethylpropanoic acid), a novel, orally active leukotriene biosynthesis inhibitor
Published in Canadian journal of physiology and pharmacology (01-05-1989)“…L-663,536 (3-[1-(4-chlorobenzyl)-3-t-butyl-thio-5-isopropylindol-2-yl]-2, 2-dimethylpropanoic acid) is a potent inhibitor of leukotriene (LT) biosynthesis in…”
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8
Arachidonic acid metabolism in purified human lung mast cells
Published in The Journal of immunology (1950) (01-04-1984)“…Arachidonic acid metabolism has been explored in preparations of purified human lung mast cells prelabeled with arachidonic acid (AA). Cells were of 83 to…”
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Prostaglandin D2 is a potent chemoattractant for human eosinophils that acts via a novel DP receptor
Published in Blood (15-09-2001)“…Prostaglandin D2 (PGD2) is released following exposure of asthmatics to allergen and acts via the adenylyl cyclase–coupled receptor for PGD2 (DP receptor). In…”
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Quantification of Lipid Mediator Metabolites in Human Urine from Asthma Patients by Electrospray Ionization Mass Spectrometry: Controlling Matrix Effects
Published in Analytical chemistry (Washington) (20-08-2013)“…Eicosanoids (e.g., prostaglandins and leukotrienes) are inflammatory signaling molecules that are metabolized and excreted in urine. The quantification of…”
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Effects of metabolites of leukotriene B4 on human neutrophil migration and cytosolic calcium levels
Published in The Journal of pharmacology and experimental therapeutics (01-02-1996)“…Leukotriene B4 (LTB4) is metabolized by beta-oxidation, omega-oxidation and the 12-hydroxyeicosanoid dehydrogenase/delta 10-reductase pathway. We have…”
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Measuring leukotrienes of slow reacting substance of anaphylaxis: development of a specific radioimmunoassay
Published in The Journal of immunology (1950) (01-07-1983)“…Rabbits were immunized with leukotriene C4 (LTC4) coupled to thiolated keyhole limpet hemocyanin (KLH) by using 6-N-maleimidohexanoic acid as a spacer…”
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Development of a novel series of styrylquinoline compounds as high-affinity leukotriene D4 receptor antagonists: synthetic and structure-activity studies leading to the discovery of (.+-.)-3-[[[3-[2-(7-chloro-2-quinolinyl)-(E)-ethenyl]phenyl][[3-(dimethylamino)-3-oxopropyl]thio]methyl]thio]propionic acid
Published in Journal of medicinal chemistry (01-10-1992)“…Based on LTD4 receptor antagonist activity of 3-(2-quinolinyl-(E)-ethenyl)pyridine (2) found in broad screening, structure-activity studies were carried out…”
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Increased F 2 ‐isoprostanes in Alzheimer's disease: evidence for enhanced lipid peroxidation in vivo
Published in The FASEB journal (01-12-1998)Get full text
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Stereochemical requirements for substrate specificity of LTB4 20-hydroxylase
Published in The Journal of biological chemistry (15-09-1987)“…LTB4 20-hydroxylase (P-450LTB) is the cytochrome P-450 in the microsomes of human polymorphonuclear leukocytes that catalyzes the omega-oxidation of…”
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Isoprostanes: Formation, Analysis and Use As Indices of Lipid Peroxidation in Vivo
Published in The Journal of biological chemistry (27-08-1999)Get full text
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Vitamin E suppresses isoprostane generation in vivo and reduces atherosclerosis in ApoE-deficient mice
Published in Nature medicine (01-10-1998)“…Oxidative modification of low density lipoprotein (LDL) has been implicated in atherogenesis. Evidence consistent with this hypothesis includes the presence of…”
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Effects of Vitamin E on Lipid Peroxidation in Healthy Persons
Published in JAMA : the journal of the American Medical Association (07-03-2001)“…CONTEXT Oxidative stress may play a role in the development or exacerbation of many common diseases. However, results of prospective controlled trials of the…”
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Chronic melatonin therapy fails to alter amyloid burden or oxidative damage in old Tg2576 mice: implications for clinical trials
Published in Brain research (10-03-2005)“…Melatonin has been proposed as a treatment for Alzheimer's disease based on the demonstration of antioxidant and “anti-amyloid” effects in vitro and in vivo…”
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Enhanced formation of 5-oxo-6,8,11,14-eicosatetraenoic acid by cancer cells in response to oxidative stress, docosahexaenoic acid and neutrophil-derived 5-hydroxy-6,8,11,14-eicosatetraenoic acid
Published in Carcinogenesis (New York) (01-06-2011)“…The 5-lipoxygenase (5-LO) product 5-oxo-6,8,11,14-eicosatetraenoic acid (5-oxo-ETE), which is a potent chemoattractant for myeloid cells, is known to promote…”
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