Page last updated: 2024-08-17

nad and 2-amino-4-hydroxy-6-formylpteridine

nad has been researched along with 2-amino-4-hydroxy-6-formylpteridine in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's6 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Arai, T; Endo, N; Fukuda, K; Hirota, K; Ishii, H; Makino, K; Mori, H; Sasada, M; Yamashita, K1
Arai, T; Endo, N; Kodaki, T; Makino, K; Nonogawa, M; Pack, SP1
Arai, T; Endo, N; Kodaki, T; Makino, K; Nonogawa, M; Pack, SP; Piyanart, S1
Arai, T; Endo, N; Kodaki, T; Makino, K; Nonogawa, M; Pack, SP; Sommani, P1
Arai, T; Endo, N; Kodaki, T; Kotake, Y; Makino, K; Nonogawa, M; Pack, SP; Sommani, P2

Other Studies

6 other study(ies) available for nad and 2-amino-4-hydroxy-6-formylpteridine

ArticleYear
6-formylpterin, a xanthine oxidase inhibitor, intracellularly generates reactive oxygen species involved in apoptosis and cell proliferation.
    Free radical biology & medicine, 2001, Feb-01, Volume: 30, Issue:3

    Topics: Apoptosis; Catalase; Cell Division; Chelating Agents; Chromatography, High Pressure Liquid; Deferoxamine; Electrochemistry; Electron Spin Resonance Spectroscopy; Enzyme Inhibitors; fas Receptor; HL-60 Cells; Humans; Hydrogen Peroxide; Jurkat Cells; NAD; Nucleotides; Oxidation-Reduction; Oxygen Consumption; Pteridines; Pterins; Reactive Oxygen Species; Superoxides; Xanthine Oxidase

2001
Novel 6-formylpterin derivatives: chemical synthesis and O2 to ROS conversion activities.
    Organic & biomolecular chemistry, 2006, May-07, Volume: 4, Issue:9

    Topics: Electrodes; NAD; Neuroprotective Agents; Oxidation-Reduction; Oxygen; Pterins; Reactive Oxygen Species; Solubility; Structure-Activity Relationship; Ultraviolet Rays

2006
Chemical natures and application of 6-formylpterin derivatives.
    Nucleic acids symposium series (2004), 2006, Issue:50

    Topics: Darkness; NAD; Oxidation-Reduction; Pterins

2006
Reactive oxygen species generation through NADH oxidation by 6-formylpterin derivatives in the dark.
    Biochemical and biophysical research communications, 2007, Feb-23, Volume: 353, Issue:4

    Topics: Darkness; Electron Spin Resonance Spectroscopy; Hydrogen Peroxide; Molecular Structure; NAD; Oxidation-Reduction; Oxygen; Pterins; Reactive Oxygen Species; Time Factors

2007
Synthesis of 6-formylpterin nucleoside analogs and their ROS generation activities in the presence of NADH in the dark.
    Organic & biomolecular chemistry, 2007, Oct-21, Volume: 5, Issue:20

    Topics: Darkness; Electron Spin Resonance Spectroscopy; NAD; Nucleosides; Pterins; Reactive Oxygen Species

2007
Chemical natures of 6-formylpterin nucleoside analogs.
    Nucleic acids symposium series (2004), 2007, Issue:51

    Topics: Electron Spin Resonance Spectroscopy; NAD; Nucleosides; Pterins; Reactive Oxygen Species

2007