Page last updated: 2024-08-18

2-naphthol and hydroquinone

2-naphthol has been researched along with hydroquinone in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19902 (40.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dunn, WJ; Grigoras, S; Koehler, MG1
Strassburg, CP; Tukey, RH1
HECKER, E; MUELLER, GC1
Chung, HY; Chung, SW; Ha, YM; Lee, H; Song, S; Suh, H1
Fahs, Z; Grimaldi, S; Guigliarelli, B; Hajj Chehade, M; Magalon, A; Pierrel, F; Pilet, E; Rendon, J; Seduk, F; Sylvi, L1

Reviews

1 review(s) available for 2-naphthol and hydroquinone

ArticleYear
Human UDP-glucuronosyltransferases: metabolism, expression, and disease.
    Annual review of pharmacology and toxicology, 2000, Volume: 40

    Topics: Autoimmunity; Chromosome Mapping; Glucuronides; Glucuronosyltransferase; Humans; Hyperbilirubinemia; Neoplasms; Steroids; Terminology as Topic

2000

Other Studies

4 other study(ies) available for 2-naphthol and hydroquinone

ArticleYear
The role of solvent-accessible surface area in determining partition coefficients.
    Journal of medicinal chemistry, 1987, Volume: 30, Issue:7

    Topics: Diffusion; Solubility; Solvents; Structure-Activity Relationship

1987
Formation of tetralin-p-quinol and a protein-bound derivative from tetrahydro-2-naphthol-8-C14 by rat liver microsomes.
    The Journal of biological chemistry, 1958, Volume: 233, Issue:4

    Topics: Animals; Hydroquinones; Liver; Microsomes; Microsomes, Liver; Naphthalenes; Naphthols; Rats; Tetrahydronaphthalenes

1958
4-(6-Hydroxy-2-naphthyl)-1,3-bezendiol: a potent, new tyrosinase inhibitor.
    Biological & pharmaceutical bulletin, 2007, Volume: 30, Issue:9

    Topics: Agaricales; Animals; Cell Survival; Dose-Response Relationship, Drug; Enzyme Inhibitors; Hydroquinones; Kinetics; Melanins; Melanoma, Experimental; Mice; Monophenol Monooxygenase; Naphthalenes; Naphthols; Phenols; Pyrones; Resorcinols; Resveratrol; Stilbenes

2007
Demethylmenaquinol is a substrate of Escherichia coli nitrate reductase A (NarGHI) and forms a stable semiquinone intermediate at the NarGHI quinol oxidation site.
    Biochimica et biophysica acta, 2015, Volume: 1847, Issue:8

    Topics: Benzoquinones; Cell Respiration; Electron Spin Resonance Spectroscopy; Escherichia coli; Hydroquinones; Kinetics; Naphthols; Nitrate Reductase; Nitrates; Oxidation-Reduction; Vitamin K 2

2015