Page last updated: 2024-08-21

equilenin and nadp

equilenin has been researched along with nadp in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's0 (0.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Alam, Z; Bolton, JL; Huang, Z; Krol, E; Pezzuto, JM; Pisha, E; Shen, L; van Breemen, RB1
Kurosawa, T; Liehr, JG; Sarabia, SF; Tohma, M; Zhu, BT1
Bolton, JL; Chandrasena, ER; Peng, KW; Thatcher, GR; van Breemen, RB; Wang, Z; Yuan, Y1
Bolton, JL; Chang, M; Peng, KW; Qin, Z; Thatcher, GR; Wang, YT; Wang, Z1

Other Studies

4 other study(ies) available for equilenin and nadp

ArticleYear
Bioreductive activation of catechol estrogen-ortho-quinones: aromatization of the B ring in 4-hydroxyequilenin markedly alters quinoid formation and reactivity.
    Carcinogenesis, 1997, Volume: 18, Issue:5

    Topics: Animals; Equilenin; Estrogens, Catechol; Humans; Kinetics; Melanoma; Microsomes, Liver; NAD(P)H Dehydrogenase (Quinone); NADP; Oxidation-Reduction; Oxygen Consumption; Quinones; Rats; Tumor Cells, Cultured

1997
Mechanism of cytochrome P450-catalyzed aromatic hydroxylation of estrogens.
    Chemical research in toxicology, 1997, Volume: 10, Issue:7

    Topics: Animals; Cricetinae; Cytochrome P-450 Enzyme System; Equilenin; Estrogens; Estrone; Hydroxylation; In Vitro Techniques; Kinetics; Male; Mesocricetus; Microsomes, Liver; NADP; Naphthols; Proadifen

1997
Redox cycling of catechol estrogens generating apurinic/apyrimidinic sites and 8-oxo-deoxyguanosine via reactive oxygen species differentiates equine and human estrogens.
    Chemical research in toxicology, 2010, Aug-16, Volume: 23, Issue:8

    Topics: 8-Hydroxy-2'-Deoxyguanosine; Animals; Cattle; Cell Line, Tumor; Chelating Agents; Copper; Deoxyguanosine; DNA; DNA Damage; DNA, Neoplasm; Equilenin; Estrogens, Catechol; Free Radical Scavengers; Horses; Humans; Hydrogen Peroxide; Hydroxyestrones; Molecular Structure; NADP; Oxidation-Reduction; Reactive Oxygen Species; Structure-Activity Relationship

2010
Unexpected hormonal activity of a catechol equine estrogen metabolite reveals reversible glutathione conjugation.
    Chemical research in toxicology, 2010, Aug-16, Volume: 23, Issue:8

    Topics: Animals; Cell Proliferation; DNA, Neoplasm; Equilenin; Glutathione; Horses; Humans; Ligands; NADP; Receptors, Estrogen; Sulfhydryl Compounds; Tumor Cells, Cultured

2010
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