kojic acid has been researched along with stilbenes in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 6 (46.15) | 29.6817 |
| 2010's | 6 (46.15) | 24.3611 |
| 2020's | 1 (7.69) | 2.80 |
| Authors | Studies |
|---|---|
| Kim, Y; Kim, YM; Lee, CK; Lee, H; Min, KR; Yun, J | 1 |
| Akao, Y; Iinuma, M; Iliya, I; Ito, T; Matsumoto, K; Nozawa, Y; Ohguchi, K; Tanaka, T | 1 |
| Akao, Y; Iinuma, M; Ito, T; Matsumoto, K; Nozawa, Y; Ohguchi, K; Tanaka, T | 1 |
| Bae, S; Chung, HY; Ha, YM; Jin, Y; Lee, H; Song, S; Suh, H | 1 |
| Chung, HY; Chung, SW; Ha, YM; Lee, H; Song, S; Suh, H | 1 |
| Kim, YJ; Yokozawa, T | 1 |
| Bae, SJ; Choi, J; Chung, HY; Ha, YM; Lee, EK; Lee, H; Lee, JS; No, JK; Song, S; Suh, H; Yu, BP | 1 |
| Tan, HY; Wang, M; Zheng, ZP | 1 |
| Aligiannis, N; Chaita, E; Lambrinidis, G; Makropoulou, M; Mikros, E; Skaltsounis, AL; Vontzalidou, A; Zoidis, G | 1 |
| Bae, SJ; Chun, P; Chung, HY; Ha, TK; Ha, YM; Kim, JA; Moon, HR; Park, D; Park, JY; Park, NH | 1 |
| da Silva, AD; da Silva, AF; do Carmo, AM; Lima, LL; Lima, RM; Raposo, NR | 1 |
| Akter, J; Chun, P; Kang, D; Lee, S; Moon, HR; Park, C; Park, Y; Ullah, S; Yang, J | 1 |
| Liu, X; Qiu, F; Rao, J; Wang, K; Wang, M; Yao, T | 1 |
13 other study(ies) available for kojic acid and stilbenes
| Article | Year |
|---|---|
Oxyresveratrol and hydroxystilbene compounds. Inhibitory effect on tyrosinase and mechanism of action.
Topics: Agaricales; Animals; Antioxidants; Enzyme Inhibitors; Gene Expression Regulation, Enzymologic; Kinetics; Melanoma, Experimental; Mice; Monophenol Monooxygenase; Plant Extracts; Promoter Regions, Genetic; Pyrones; Stilbenes; Structure-Activity Relationship; Tumor Cells, Cultured | 2002 |
Gnetol as a potent tyrosinase inhibitor from genus Gnetum.
Topics: Animals; Gnetum; Inhibitory Concentration 50; Melanins; Melanoma, Experimental; Mice; Peptides; Pyrones; Stilbenes | 2003 |
Inhibitory effects of resveratrol derivatives from dipterocarpaceae plants on tyrosinase activity.
Topics: Animals; Cell Line, Tumor; Enzyme Inhibitors; Ericales; Mice; Molecular Structure; Monophenol Monooxygenase; Pyrones; Resveratrol; Stilbenes; Structure-Activity Relationship | 2003 |
Syntheses of hydroxy substituted 2-phenyl-naphthalenes as inhibitors of tyrosinase.
Topics: Agaricales; Crystallography, X-Ray; Dealkylation; Enzyme Inhibitors; Hydroquinones; Indicators and Reagents; Magnetic Resonance Spectroscopy; Mass Spectrometry; Models, Molecular; Monophenol Monooxygenase; Morus; Naphthalenes; Pyrones; Resveratrol; Stilbenes | 2007 |
4-(6-Hydroxy-2-naphthyl)-1,3-bezendiol: a potent, new tyrosinase inhibitor.
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 |
Piceatannol inhibits melanogenesis by its antioxidative actions.
Topics: Animals; Antioxidants; Cell Line, Tumor; Dose-Response Relationship, Drug; Down-Regulation; Glutathione; Glutathione Disulfide; Inhibitory Concentration 50; Melanins; Melanocytes; Melanoma, Experimental; Mice; Molecular Structure; Monophenol Monooxygenase; Pyrones; Reactive Oxygen Species; Resveratrol; Stilbenes | 2007 |
A newly synthesized, potent tyrosinase inhibitor: 5-(6-hydroxy-2-naphthyl)-1,2,3-benzenetriol.
Topics: Agaricales; Animals; Enzyme Inhibitors; Kinetics; Melanins; Melanoma, Experimental; Mice; Monophenol Monooxygenase; Naphthols; Pyrogallol; Pyrones; Resveratrol; Stilbenes | 2010 |
Tyrosinase inhibition constituents from the roots of Morus australis.
Topics: Agaricales; Benzofurans; Chromatography, High Pressure Liquid; Enzyme Inhibitors; Heterocyclic Compounds, 4 or More Rings; Molecular Structure; Monophenol Monooxygenase; Morus; Phenols; Plant Extracts; Plant Roots; Plant Stems; Pyrones; Resveratrol; Stilbenes | 2012 |
Design, synthesis and molecular simulation studies of dihydrostilbene derivatives as potent tyrosinase inhibitors.
Topics: Bacteria; Benzoin; Drug Design; Enzyme Inhibitors; Fungi; Molecular Docking Simulation; Monophenol Monooxygenase; Pyrones; Stilbenes; Structure-Activity Relationship | 2012 |
A novel synthesized tyrosinase inhibitor: (E)-2-((2,4-dihydroxyphenyl)diazenyl)phenyl 4-methylbenzenesulfonate as an azo-resveratrol analog.
Topics: Animals; Azo Compounds; Benzenesulfonates; Cell Line, Tumor; Cell Survival; Dose-Response Relationship, Drug; Enzyme Assays; Enzyme Inhibitors; Fungal Proteins; Kinetics; Melanins; Melanoma, Experimental; Mice; Molecular Docking Simulation; Monophenol Monooxygenase; Pigmentation Disorders; Pyrones; Resveratrol; Stilbenes | 2013 |
Azastilbene analogs as tyrosinase inhibitors: new molecules with depigmenting potential.
Topics: Agaricales; Antioxidants; Enzyme Inhibitors; Fungal Proteins; Molecular Conformation; Monophenol Monooxygenase; Phenols; Pyrones; Resveratrol; Stilbenes; Structure-Activity Relationship; Time Factors | 2013 |
Antioxidant, anti-tyrosinase and anti-melanogenic effects of (E)-2,3-diphenylacrylic acid derivatives.
Topics: Agaricus; Animals; Catalytic Domain; Cell Line, Tumor; Cinnamates; Enzyme Inhibitors; Free Radical Scavengers; Mice; Molecular Docking Simulation; Monophenol Monooxygenase; Protein Binding; Pyrones; Skin Lightening Preparations; Stilbenes | 2019 |
Highly Potent Inhibition of Tyrosinase by Mulberrosides and the Inhibitory Mechanism in Vitro.
Topics: Binding Sites; Enzyme Inhibitors; Glycosides; Inhibitory Concentration 50; Kinetics; Molecular Docking Simulation; Monophenol Monooxygenase; Morus; Protein Structure, Tertiary; Pyrones; Stilbenes | 2022 |