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2,2,5,7,8-pentamethyl-1-hydroxychroman and butylated hydroxytoluene

2,2,5,7,8-pentamethyl-1-hydroxychroman has been researched along with butylated hydroxytoluene in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aizawa, Y; Hasegawa, K; Iizuka, Y; Iwaoka, T; Kanai, T; Yamaguchi, T; Yoshioka, T1
Aragno, M; Boschi, D; Cena, C; Chegaev, K; Di Stilo, A; Fruttero, R; Gasco, A; Lazzarato, L; Tron, GC1
Bertinaria, M; Boschi, D; Cena, C; Chegaev, K; Di Stilo, A; Fruttero, R; Gasco, A; Giorgis, M; Lazzarato, L; Tron, GC1

Other Studies

3 other study(ies) available for 2,2,5,7,8-pentamethyl-1-hydroxychroman and butylated hydroxytoluene

ArticleYear
Studies on hindered phenols and analogues. 2. 1,3-Benzoxathioles having SRS-A inhibiting activity.
    Journal of medicinal chemistry, 1990, Volume: 33, Issue:5

    Topics: Animals; Asthma; Benzoxazoles; Chemical Phenomena; Chemistry; Guinea Pigs; Lipid Peroxidation; Lipoxygenase Inhibitors; Mice; Mice, Inbred C57BL; SRS-A; Structure-Activity Relationship

1990
Development of a new class of potential antiatherosclerosis agents: NO-donor antioxidants.
    Bioorganic & medicinal chemistry letters, 2004, Dec-20, Volume: 14, Issue:24

    Topics: Animals; Antioxidants; Aorta; Arteriosclerosis; Ascorbic Acid; Ferrous Compounds; Hepatocytes; Hypolipidemic Agents; Lipid Peroxidation; Male; Membrane Lipids; Nitric Oxide Donors; Phenols; Phenylephrine; Rats; Rats, Wistar; Structure-Activity Relationship; Thiobarbituric Acid Reactive Substances

2004
NO-donor phenols: a new class of products endowed with antioxidant and vasodilator properties.
    Journal of medicinal chemistry, 2006, May-18, Volume: 49, Issue:10

    Topics: Animals; Antioxidants; Aorta, Thoracic; In Vitro Techniques; Lipid Metabolism; Male; Microsomes, Liver; Muscle Contraction; Muscle, Smooth, Vascular; Nitrates; Nitric Oxide Donors; Oxadiazoles; Oxidation-Reduction; Phenols; Rats; Rats, Wistar; Structure-Activity Relationship; Thiobarbituric Acid Reactive Substances; Vasodilator Agents

2006