2,2'-azobis(2-amidinopropane) and eicosapentaenoic acid

2,2'-azobis(2-amidinopropane) has been researched along with eicosapentaenoic acid in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (75.00)18.2507
2000's1 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Anti, M; Armelao, F; Bartoli, GM; Franceschelli, P; Luberto, C; Marra, G; Palozza, P; Piccioni, E; Sgarlata, E1
Niki, E; Ukegawa, K; Yamamoto, Y; Yazu, K1
AnggÄrd, EE; Halliwell, B; Nourooz-Zadeh, J1
Brooks, JD; Milne, GL; Morrow, JD; Porter, NA; Sanchez, SC; Yin, H1

Trials

1 trial(s) available for 2,2'-azobis(2-amidinopropane) and eicosapentaenoic acid

ArticleYear
n-3 fatty acids induce oxidative modifications in human erythrocytes depending on dose and duration of dietary supplementation.
    The American journal of clinical nutrition, 1996, Volume: 64, Issue:3

    Topics: Adult; Amidines; Dietary Fats; Docosahexaenoic Acids; Dose-Response Relationship, Drug; Eicosapentaenoic Acid; Erythrocyte Membrane; Fatty Acids, Omega-3; Female; Food, Fortified; Humans; Lipid Peroxides; Male; Middle Aged; Oxidation-Reduction; Time Factors; Vitamin E

1996

Other Studies

3 other study(ies) available for 2,2'-azobis(2-amidinopropane) and eicosapentaenoic acid

ArticleYear
Mechanism of lower oxidizability of eicosapentaenoate than linoleate in aqueous micelles.
    Lipids, 1996, Volume: 31, Issue:3

    Topics: Amidines; Azo Compounds; Chlorobenzenes; Eicosapentaenoic Acid; Esters; Fatty Acids, Unsaturated; Kinetics; Linoleic Acid; Linoleic Acids; Micelles; Models, Chemical; Nitriles; Octoxynol; Oxidation-Reduction; Peroxides

1996
Evidence for the formation of F3-isoprostanes during peroxidation of eicosapentaenoic acid.
    Biochemical and biophysical research communications, 1997, Jul-18, Volume: 236, Issue:2

    Topics: Amidines; Copper; Dinoprost; Eicosapentaenoic Acid; Gas Chromatography-Mass Spectrometry; Lipid Peroxides; Liposomes; Prostaglandins F

1997
Formation of highly reactive cyclopentenone isoprostane compounds (A3/J3-isoprostanes) in vivo from eicosapentaenoic acid.
    The Journal of biological chemistry, 2008, May-02, Volume: 283, Issue:18

    Topics: Amidines; Animals; Catalysis; Dietary Supplements; Eicosapentaenoic Acid; Fish Oils; Gas Chromatography-Mass Spectrometry; Glutathione; Hydrogenation; Isomerism; Isoprostanes; Liver; Oxidation-Reduction; Phospholipids; Rats; Spectrometry, Mass, Electrospray Ionization; Time Factors

2008