ascorbic-acid and ethylenediamine

ascorbic-acid has been researched along with ethylenediamine* in 4 studies

Other Studies

4 other study(ies) available for ascorbic-acid and ethylenediamine

ArticleYear
Antioxidant and anti-aging carbon quantum dots using tannic acid.
    Nanotechnology, 2021, Jul-23, Volume: 32, Issue:41

    Overexpression of collagenase, elastase, and tyrosinase is caused by external factors such as ultraviolet (UV) radiation and stress, resulting in wrinkle formation and freckles through the loss of skin elasticity and skin pigmentation. In this study, we developed novel carbon quantum dots (CQDs) with antioxidant and anti-aging properties using tannic acid as a carbon source through a simple microwave-assisted pyrolysis method. The synthesized tannic acid-derived CQDs (T-CQDs) showed bright blue fluorescence (QY = 28.2 ± 4.0%), exhibiting maximum emission at 430 nm under 350 nm excitation. Even though small amount of the T-CQDs (3

    Topics: Antioxidants; Ascorbic Acid; Biphenyl Compounds; Carbon; Cell Line, Tumor; Cell Survival; Collagenases; Enzyme Inhibitors; Ethylenediamines; Geroscience; Humans; Melanocytes; Microwaves; Monophenol Monooxygenase; Pancreatic Elastase; Picrates; Quantum Dots; Quercetin; Tannins

2021
Metabolic activation of 1-naphthol by rat liver microsomes to 1,4-naphthoquinone and covalent binding species.
    Biochemical pharmacology, 1984, Oct-15, Volume: 33, Issue:20

    1-Naphthol was metabolized by rat liver microsomes, in the presence of an NADPH-generating system, both to methanol-soluble metabolites including 1,4-naphthoquinone and an uncharacterized product(s) (X) and also to covalently bound products. NADH was much less effective as an electron donor than NADPH. Metyrapone, SKF 525-A and carbon monoxide all inhibited the metabolism of 1-naphthol to 1,4-naphthoquinone and to covalently bound products suggesting the involvement of cytochrome P-450 in at least one step in the metabolic activation of 1-naphthol to reactive products. Ethylene diamine, which reacts selectively with 1,2-naphthoquinone but not 1,4-naphthoquinone, did not affect the covalent binding whereas glutathione, which reacts with both naphthoquinones, caused an almost total inhibition of covalent binding. These and other results suggested that 1,4-naphthoquinone, or a metabolite derived from it, was responsible for most of the covalent binding observed and that little if any of the binding was due to 1,2-naphthoquinone.

    Topics: Animals; Ascorbic Acid; Biotransformation; Cytochrome P-450 Enzyme System; Ethylenediamines; Glutathione; In Vitro Techniques; Male; Microsomes, Liver; Naphthols; Naphthoquinones; Rats; Rats, Inbred Strains; Superoxide Dismutase

1984
[ORGANIC CATALYSTS, LXXV. CHELATE CATALYSIS, 18. ON REACTION INACTIVATION OF ASCORBIC ACID OXIDATION CATALYZED BY COBALT-N,N'-BIS-(5-SULFOSALICYLIDENE)-ETHYLENEDIAMINE].
    Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 1965, Volume: 340

    Topics: Ascorbic Acid; Catalysis; Cobalt; Dehydroascorbic Acid; Ethylenediamines; Oxidation-Reduction; Research

1965
[Effect of combined theophylline-ethylenediamine, rutin and ascorbic acid in therapy of cerebral apoplexy; early clinico-therapeutic results].
    Minerva medica, 1955, Jun-09, Volume: 46, Issue:46

    Topics: Aminophylline; Ascorbic Acid; Cerebral Hemorrhage; Ethylenediamines; Flavonoids; Humans; Rutin; Stroke; Theophylline; Vitamins

1955