linoleic-acid-hydroperoxide and phenidone

linoleic-acid-hydroperoxide has been researched along with phenidone* in 1 studies

Other Studies

1 other study(ies) available for linoleic-acid-hydroperoxide and phenidone

Article	Year
Soybean lipoxygenase-catalyzed oxidations by linoleic acid hydroperoxide: different reducing substrates and dehydrogenation of phenidone and BW 755C. Biochemical and biophysical research communications, 1988, Feb-29, Volume: 151, Issue:1 Phenidone is not a substrate for dioxygenation by soybean lipoxygenase-1 (L1) but reduces L1Fe(III) into L1Fe(II), as shown by EPR spectroscopy. L1 catalyzes the oxidation of phenidone by 13-HPOD, the hydroperoxide formed by dioxygenation of linoleic acid by L1, with formation of 4,5-dehydrophenidone. Two moles of 13-HPOD are used per mole of phenidone dehydrogenated. Other pyrazoline derivatives such as BW 755C, but also, in a more general manner, different compounds containing phenol, aniline, hydrazine, hydroxylamine or hydrazide functions act as reducing substrates for decomposition of 13-HPOD by L1. Topics: 4,5-Dihydro-1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amine; Catalysis; Chemical Phenomena; Chemistry; Chromatography, High Pressure Liquid; Glycine max; Linoleic Acids; Lipid Peroxides; Lipoxygenase; Oxidation-Reduction; Pyrazoles; Spectrophotometry, Ultraviolet; Substrate Specificity	1988

Article

Year

Soybean lipoxygenase-catalyzed oxidations by linoleic acid hydroperoxide: different reducing substrates and dehydrogenation of phenidone and BW 755C.

Biochemical and biophysical research communications, 1988, Feb-29, Volume: 151, Issue:1

Phenidone is not a substrate for dioxygenation by soybean lipoxygenase-1 (L1) but reduces L1Fe(III) into L1Fe(II), as shown by EPR spectroscopy. L1 catalyzes the oxidation of phenidone by 13-HPOD, the hydroperoxide formed by dioxygenation of linoleic acid by L1, with formation of 4,5-dehydrophenidone. Two moles of 13-HPOD are used per mole of phenidone dehydrogenated. Other pyrazoline derivatives such as BW 755C, but also, in a more general manner, different compounds containing phenol, aniline, hydrazine, hydroxylamine or hydrazide functions act as reducing substrates for decomposition of 13-HPOD by L1.

Topics: 4,5-Dihydro-1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amine; Catalysis; Chemical Phenomena; Chemistry; Chromatography, High Pressure Liquid; Glycine max; Linoleic Acids; Lipid Peroxides; Lipoxygenase; Oxidation-Reduction; Pyrazoles; Spectrophotometry, Ultraviolet; Substrate Specificity

1988