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MedChemExpress
kojic acid ![]() Kojic Acid, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/kojic+acid/Kojic+acid/pmc13028802-167-13-25 Average 94 stars, based on 1 article reviews
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Chem Impex International
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Selleck Chemicals
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Valiant Co Ltd
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Merck KGaA
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Novozymes limited
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Biometec Inc
alginic-kojic acid material ![]() Alginic Kojic Acid Material, supplied by Biometec Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/kojic+acid/alginic+kojic+acid+material/pm39111504-10-2-67 Average 90 stars, based on 1 article reviews
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FUJIFILM
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Sansho Seiyaku Co
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Panapharm Laboratories
kojic acid ![]() Kojic Acid, supplied by Panapharm Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/kojic+acid/kojic+acid/pm12700405-1-109-83 Average 90 stars, based on 1 article reviews
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Carl Roth GmbH
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ChemFaces Biochemical Co Ltd
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Image Search Results
Journal: Pharmaceuticals
Article Title: Glabridin Inhibits Melanogenesis and Melanin Transfer via Wnt/β-Catenin Pathway and Rho Family GTPase-Mediated Dendritic Formation Suppression
doi: 10.3390/ph19030469
Figure Lengend Snippet: Effect of glabridin on anti-melanogenesis. Different concentrations of glabridin on MNT-1 cell viability ( a ) and on HaCaT cell viability ( b ), assessed by the MTT assay; Different concentrations of niacinamide on MNT-1 cell viability ( c ) and on HaCaT cell viability ( d ), assessed by the MTT assay; ( e ) Glabridin inhibit melanin content in MNT-1 cells. ( f ) Glabridin inhibit intracellular tyrosinase activity in MNT-1 cells. The images of protein bands ( g ) and the relative protein levels of MITF ( h ), TYR ( i ), TRP-1 ( j ) and TRP-2 ( k ). GAPDH served as the internal control. Kojic acid (KA, 200 μg/mL) was used as a positive control. Data are presented as mean ± SD ( n = 3) (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. control) (one-way ANOVA followed by Tukey’s post hoc test).
Article Snippet: After 60 h incubation, In the anti-melanogenesis assay, different concentrations of glabridin and
Techniques: MTT Assay, Activity Assay, Control, Positive Control
Journal: International Journal of Molecular Sciences
Article Title: Inhibition of NAT10 Suppresses Melanogenesis and Melanoma Growth by Attenuating Microphthalmia-Associated Transcription Factor (MITF) Expression
doi: 10.3390/ijms18091924
Figure Lengend Snippet: Effect of remodelin on melanin synthesis in B16F10 mouse melanoma cells. ( A ) Remodelin suppressed α-melanocyte-stimulating hormone (α-MSH)-induced melanin synthesis. Cells were pre-incubated in the absence or presence of remodelin for 1 h, followed by their incubation with α-MSH (0.2 mM) for 3 days. α-MSH increased the extracellular and intracellular melanin content; however, remodelin treatment decreased these levels. Color changes in the cultured medium are shown. Values represent mean ± SD of three independent experiments performed in triplicates; ** p < 0.01, # p < 0.05, and ## p < 0.01; ( B ) Inhibitory effect of remodelin on cellular tyrosinase activity. Tyrosinase activity was determined by measuring l -DOPA (2 mM) oxidation to dopachrome at 475 nm (OD475). Values represent mean ± SD of three independent experiments performed in duplicates; * p < 0.05 and ** p < 0.01; ( C ) Effect of remodelin on MITF, TYR, and DCT mRNA expression levels was measured using quantitative RT-PCR. Values represent mean ± SD of three independent experiments performed in duplicates; * p < 0.05 and ** p < 0.01; ( D ) Effect of remodelin on MITF and tyrosinase protein levels. B16F10 cells were pre-incubated with arbutin, kojic acid, or remodelin for 1 h, followed by their treatment with α-MSH for 12 h. MITF and tyrosinase protein expression levels were measured by western blotting.
Article Snippet: Remodelin (S7641), α-MSH (M4135), arbutin (A4256),
Techniques: Incubation, Cell Culture, Activity Assay, Expressing, Quantitative RT-PCR, Western Blot
Journal: Molecules
Article Title: Timeline of the Development of Skin-Lightening Active Ingredients in Japan
doi: 10.3390/molecules27154774
Figure Lengend Snippet: List of skin-lightening active ingredients approved in Japan.
Article Snippet: 1988 ,
Techniques: Inhibition
Journal: Molecules
Article Title: Timeline of the Development of Skin-Lightening Active Ingredients in Japan
doi: 10.3390/molecules27154774
Figure Lengend Snippet: Comparison of clinical trials of skin-lightening agents and drugs for the treatment of age spots.
Article Snippet: 1988 ,
Techniques: Comparison, Clinical Proteomics, Formulation
Journal: Heliyon
Article Title: Synergistic effects of novel herbal decoctions from Panax ginseng and Morus alba on tyrosinase activity and melanogenesis in vitro
doi: 10.1016/j.heliyon.2022.e08866
Figure Lengend Snippet: Effects of herbal decoctions on melanin synthesis in B16 cells. Cells were pretreated with (A) MC and GMC or (B) MR or GMR at the indicated concentrations (0, 6.25, 12.5, and 25 μg/mL) for 1 h before exposure to forskolin (20 μM) for 6 days. Kojic acid was used as the positive control. The secreted melanin levels were analyzed by measuring absorbance using a microplate reader (420 nm). Bar graph (mean ± SEM) data from three experiments were determined using one-way ANOVA with Tukey's post hoc test, ∗∗∗P < 0.001; ∗∗P < 0.01; ∗P < 0.05, compared with the vehicle group.
Article Snippet:
Techniques: Positive Control
Journal: Heliyon
Article Title: Synergistic effects of novel herbal decoctions from Panax ginseng and Morus alba on tyrosinase activity and melanogenesis in vitro
doi: 10.1016/j.heliyon.2022.e08866
Figure Lengend Snippet: Anti-tyrosinase activity of the main components in GMC and GMR. The mushroom tyrosinase activity of tyrosinase was determined using 1 mM L-dopa as the substrate in the absence and presence of each compound: (A) kojic acid, (B) ginsenoside Rg1 (C) morusin (D) mulberroside A (E) oxyresveratrol. Bar graph (mean ± SEM) data were determined from three experiments using one-way ANOVA with Tukey's post hoc test, ∗∗∗P < 0.001; ∗∗P < 0.01; ∗P < 0.05, compared with the vehicle group.
Article Snippet:
Techniques: Activity Assay