hydrogen and 15-hydroperoxy-5,8,11,13-eicosatetraenoic acid

hydrogen has been researched along with 15-hydroperoxy-5,8,11,13-eicosatetraenoic acid in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19902 (66.67)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Brash, AR; Maas, RL; Porter, AT1
Brash, AR; Ingram, CD; Maas, RL; Oates, JA; Porter, AT; Taber, DF1
Brash, AR; Coffa, G; Gaffney, BJ; Imber, AN; Laxmikanthan, G; Maguire, BC; Schneider, C1

Other Studies

3 other study(ies) available for hydrogen and 15-hydroperoxy-5,8,11,13-eicosatetraenoic acid

ArticleYear
Investigation of the selectivity of hydrogen abstraction in the nonenzymatic formation of hydroxyeicosatetraenoic acids and leukotrienes by autoxidation.
    The Journal of biological chemistry, 1985, Apr-10, Volume: 260, Issue:7

    Topics: Arachidonic Acids; Chemical Phenomena; Chemistry, Physical; Chromatography, High Pressure Liquid; Hydrogen; Leukotriene A4; Leukotrienes; Lipid Peroxides; Stereoisomerism

1985
Investigation of the chemical conversion of hydroperoxyeicosatetraenoate to leukotriene epoxide using stereospecifically labeled arachidonic acid. Comparison with the enzymatic reaction.
    The Journal of biological chemistry, 1985, Apr-10, Volume: 260, Issue:7

    Topics: Arachidonic Acid; Arachidonic Acids; Chemical Phenomena; Chemistry, Physical; Chromatography, High Pressure Liquid; Hydrogen; Leukotriene A4; Leukotrienes; Lipid Peroxides; Magnetic Resonance Spectroscopy; Spectrophotometry, Ultraviolet; Stereoisomerism

1985
On the relationships of substrate orientation, hydrogen abstraction, and product stereochemistry in single and double dioxygenations by soybean lipoxygenase-1 and its Ala542Gly mutant.
    The Journal of biological chemistry, 2005, Nov-18, Volume: 280, Issue:46

    Topics: Alanine; Arachidonic Acid; Binding Sites; Catalysis; Chromatography, Gas; Chromatography, High Pressure Liquid; Cloning, Molecular; DNA Primers; Dose-Response Relationship, Drug; Electron Spin Resonance Spectroscopy; Esters; Glycine; Glycine max; Hydrogen; Hydrogen-Ion Concentration; Iron; Kinetics; Leukotrienes; Linoleic Acid; Linoleic Acids; Lipid Peroxides; Lipoxygenase; Magnetic Resonance Spectroscopy; Magnetics; Mass Spectrometry; Models, Chemical; Models, Molecular; Mutagenesis; Mutation; Oxygen; Plasmids; Protein Binding; Protein Conformation; Protein Structure, Tertiary; Software; Stereoisomerism; Substrate Specificity; Time Factors; Ultraviolet Rays

2005