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kojic acid and B16 Melanoma

kojic acid has been researched along with B16 Melanoma in 39 studies

Research Excerpts

ExcerptRelevanceReference
" The two hydroxydaidzeins reduced melanin synthesis comparably to treatment with kojic acid, a proven whitening agent, in B16 melanoma cells."3.78Effects of ortho-dihydroxyisoflavone derivatives from Korean fermented soybean paste on melanogenesis in B16 melanoma cells and human skin equivalents. ( Bae, JH; Goh, MJ; Kim, DH; Kim, HK; Na, YJ; Park, JS, 2012)
" It also inhibited melanin production by B16 melanoma cell line and normal human melanocytes more efficiently than kojic acid."3.77Dimeric cinnamoylamide derivatives as inhibitors of melanogenesis. ( Criton, M; Le Mellay-Hamon, V, 2011)
"SF inhibited melanin synthesis in B16 melanoma cells via down-regulation of MITF and tyrosinase expression, which provides a rationale for future utilization of SF."1.62Quantitative proteomic analysis uncovers inhibition of melanin synthesis by silk fibroin via MITF/tyrosinase axis in B16 melanoma cells. ( Duan, T; Hong, M; Huang, H; Lu, Z; Wang, Y; Xiao, X; Zheng, J; Zhou, H; Zhou, Y, 2021)
"Kojic acid (KA) is a naturally occurring fungal metabolite that is utilized as a skin-lightener and antibrowning agent owing to its potent tyrosinase inhibition activity."1.46Biodegradable Kojic Acid-Based Polymers: Controlled Delivery of Bioactives for Melanogenesis Inhibition. ( Faig, JJ; Joseph, LB; Moretti, A; Nova, MJ; Smith, K; Uhrich, KE; Zhang, Y, 2017)
"Flavokawain analogs were synthesized through a Claisen-Schmidt condensation of their corresponding acetophenones and benzaldehydes and were evaluated in terms of their tyrosinase inhibitory and anti-melanogenesis activities."1.42Flavokawains B and C, melanogenesis inhibitors, isolated from the root of Piper methysticum and synthesis of analogs. ( Choi, J; Hong, YD; Jeong, HJ; Ko, J; Lee, CS; Lee, JH; Lee, S; Park, JS; Shin, SS; Yoon, KD, 2015)
"Treatment with glycine (1-16 mM) for 72 h inhibited alpha-melanocyte stimulating hormone (alpha-MSH)-induced melanogenesis in a concentration-dependent manner without any effects on cell proliferation in B16F0 melanoma cells."1.34Glycine inhibits melanogenesis in vitro and causes hypopigmentation in vivo. ( Ishii, F; Ishikawa, M; Kawase, I, 2007)

Research

Studies (39)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (2.56)18.2507
2000's10 (25.64)29.6817
2010's27 (69.23)24.3611
2020's1 (2.56)2.80

Authors

AuthorsStudies
Yamazaki, Y1
Kawano, Y1
Yamanaka, A1
Maruyama, S1
Matsuda, H3
Nakashima, S3
Oda, Y3
Nakamura, S3
Yoshikawa, M3
Thanigaimalai, P3
Lee, KC3
Bang, SC1
Lee, JH2
Yun, CY1
Roh, E3
Hwang, BY1
Kim, Y4
Jung, SH3
Xu, F1
Choi, J2
Bae, SJ3
Ha, YM5
No, JK1
Lee, EK2
Lee, JS1
Song, S2
Lee, H3
Suh, H2
Yu, BP1
Chung, HY7
Park, JY3
Park, YJ2
Park, D2
Choi, YJ1
Kim, JM1
Han, YK1
Kim, JA2
Lee, JY1
Moon, HR6
Sharma, VK2
Joo, C1
Cho, WJ1
Bandgar, BP1
Adsul, LK1
Chavan, HV1
Shringare, SN1
Korbad, BL1
Jalde, SS1
Lonikar, SV1
Nile, SH1
Shirfule, AL1
Oode, C1
Shimada, W1
Izutsu, Y1
Yokota, M1
Iwadate, T1
Nihei, K1
Jeong, HJ1
Lee, CS1
Hong, YD1
Shin, SS1
Park, JS2
Lee, S2
Yoon, KD1
Ko, J1
Liu, J1
Onishi, K1
Kawabata, M1
Miki, H1
Himuro, Y1
Wang, Y1
Duan, T1
Hong, M2
Zhou, Y1
Huang, H1
Xiao, X1
Zheng, J2
Zhou, H1
Lu, Z1
Chen, YM1
Su, WC1
Li, C1
Shi, Y1
Chen, QX1
Tang, DL1
Chen, SM1
Wang, Q1
Bang, E1
Noh, SG1
Ha, S1
Jung, HJ1
Kim, DH4
Lee, AK1
Hyun, MK1
Kang, D1
Park, C1
Ai, N1
Welsh, WJ1
Santhanam, U1
Hu, H1
Lyga, J1
Park, MH1
Kim, SJ2
Jeong, HO1
Moon, KM1
Son, S2
Kim, HR1
Kim, MJ1
Yun, HY2
Chun, P4
Je, NK1
Yokozawa, T2
Ullah, S1
Kim, YJ2
Yoo, JW1
Jung, Y1
Maack, A1
Pegard, A1
Chen, MJ1
Hung, CC2
Chen, YR1
Lai, ST1
Chan, CF1
Reddy, TL1
Garikapati, KR1
Reddy, SG1
Reddy, BV1
Yadav, JS1
Bhadra, U1
Bhadra, MP1
Faig, JJ1
Moretti, A1
Joseph, LB1
Zhang, Y1
Nova, MJ1
Smith, K1
Uhrich, KE1
Nesterov, A1
Zhao, J1
Minter, D1
Hertel, C1
Ma, W1
Abeysinghe, P1
Jia, Q1
Kai, H1
Baba, M1
Okuyama, T1
Zhang, X1
Hu, X1
Hou, A1
Wang, H1
An, SM1
Koh, JS1
Boo, YC1
Miyake, M1
Yamamoto, S1
Sano, O1
Fujii, M1
Kohno, K1
Ushio, S1
Iwaki, K1
Fukuda, S1
Criton, M1
Le Mellay-Hamon, V1
Wang, YW1
Jou, CH1
Yang, MC1
Goh, MJ1
Bae, JH1
Kim, HK1
Na, YJ1
Lajis, AF1
Hamid, M1
Ariff, AB1
Song, YM1
Ha, TK2
Park, NH1
Ohguchi, K1
Tanaka, T1
Iliya, I1
Ito, T1
Iinuma, M1
Matsumoto, K1
Akao, Y1
Nozawa, Y1
Chung, SW1
Ishikawa, M1
Kawase, I1
Ishii, F1
Kim, YM1
Yun, J1
Lee, CK1
Min, KR1
Mishima, Y1

Reviews

1 review available for kojic acid and B16 Melanoma

ArticleYear
A post melanosomal era: control of melanogenesis and melanoma growth.
    Pigment cell research, 1992, Volume: Suppl 2

    Topics: Adolescent; Animals; Boron; Boron Compounds; Cricetinae; Fatty Acids, Unsaturated; Gene Expression R

1992

Other Studies

38 other studies available for kojic acid and B16 Melanoma

ArticleYear
N-[(Dihydroxyphenyl)acyl]serotonins as potent inhibitors of tyrosinase from mouse and human melanoma cells.
    Bioorganic & medicinal chemistry letters, 2009, Aug-01, Volume: 19, Issue:15

    Topics: Animals; Antineoplastic Agents; Cell Line, Tumor; Drug Design; Drug Screening Assays, Antitumor; Enz

2009
Melanogenesis inhibitors from the rhizomes of Alpinia officinarum in B16 melanoma cells.
    Bioorganic & medicinal chemistry, 2009, Aug-15, Volume: 17, Issue:16

    Topics: Alpinia; Animals; Antineoplastic Agents; Enzyme Inhibitors; Flavonoids; Kaempferols; Melanoma, Exper

2009
Evaluation of 3,4-dihydroquinazoline-2(1H)-thiones as inhibitors of alpha-MSH-induced melanin production in melanoma B16 cells.
    Bioorganic & medicinal chemistry, 2010, Feb-15, Volume: 18, Issue:4

    Topics: alpha-MSH; Animals; Cell Line, Tumor; Drug Evaluation, Preclinical; Magnetic Resonance Spectroscopy;

2010
Melanogenesis inhibitors from the desert plant Anastatica hierochuntica in B16 melanoma cells.
    Bioorganic & medicinal chemistry, 2010, Mar-15, Volume: 18, Issue:6

    Topics: Agaricales; Animals; Antineoplastic Agents; Brassicaceae; Cell Proliferation; Cell Survival; Drug Sc

2010
A newly synthesized, potent tyrosinase inhibitor: 5-(6-hydroxy-2-naphthyl)-1,2,3-benzenetriol.
    Bioorganic & medicinal chemistry letters, 2010, Aug-15, Volume: 20, Issue:16

    Topics: Agaricales; Animals; Enzyme Inhibitors; Kinetics; Melanins; Melanoma, Experimental; Mice; Monophenol

2010
Synthesis and biological activity of hydroxy substituted phenyl-benzo[d]thiazole analogues for antityrosinase activity in B16 cells.
    Bioorganic & medicinal chemistry letters, 2011, Apr-15, Volume: 21, Issue:8

    Topics: Agaricales; Animals; Benzothiazoles; Binding Sites; Catalytic Domain; Cell Line, Tumor; Computer Sim

2011
Ketonethiosemicarbazones: structure-activity relationships for their melanogenesis inhibition.
    Bioorganic & medicinal chemistry letters, 2011, Jun-15, Volume: 21, Issue:12

    Topics: Animals; Cell Line, Tumor; Hydrophobic and Hydrophilic Interactions; Inhibitory Concentration 50; Ke

2011
Structural requirement of phenylthiourea analogs for their inhibitory activity of melanogenesis and tyrosinase.
    Bioorganic & medicinal chemistry letters, 2011, Nov-15, Volume: 21, Issue:22

    Topics: Agaricales; Animals; Catalytic Domain; Cell Line, Tumor; Enzyme Inhibitors; Humans; Melanins; Melano

2011
Synthesis, biological evaluation, and molecular docking of N-{3-[3-(9-methyl-9H-carbazol-3-yl)-acryloyl]-phenyl}-benzamide/amide derivatives as xanthine oxidase and tyrosinase inhibitors.
    Bioorganic & medicinal chemistry, 2012, Sep-15, Volume: 20, Issue:18

    Topics: Animals; Benzamides; Carbazoles; Cell Survival; Dose-Response Relationship, Drug; Enzyme Inhibitors;

2012
Synthesis of dihydroresveratrol glycosides and evaluation of their activity against melanogenesis in B16F0 melanoma cells.
    European journal of medicinal chemistry, 2014, Nov-24, Volume: 87

    Topics: Animals; Cell Line, Tumor; Drug Screening Assays, Antitumor; Glycosides; Magnetic Resonance Spectros

2014
Flavokawains B and C, melanogenesis inhibitors, isolated from the root of Piper methysticum and synthesis of analogs.
    Bioorganic & medicinal chemistry letters, 2015, Feb-15, Volume: 25, Issue:4

    Topics: Animals; Flavonoids; Humans; Kava; Melanins; Melanoma, Experimental; Mice; Structure-Activity Relati

2015
Inhibitors of melanogenesis in B16 melanoma 4A5 cells from flower buds of Lawsonia inermis (Henna).
    Bioorganic & medicinal chemistry letters, 2015, Jul-01, Volume: 25, Issue:13

    Topics: Animals; Antifibrinolytic Agents; Cell Line, Tumor; Cell Proliferation; Flavonoids; Flowers; Humans;

2015
Quantitative proteomic analysis uncovers inhibition of melanin synthesis by silk fibroin via MITF/tyrosinase axis in B16 melanoma cells.
    Life sciences, 2021, Nov-01, Volume: 284

    Topics: Animals; Fibroins; Melanins; Melanoma, Experimental; Mice; Microphthalmia-Associated Transcription F

2021
Anti-melanogenesis of novel kojic acid derivatives in B16F10 cells and zebrafish.
    International journal of biological macromolecules, 2019, Feb-15, Volume: 123

    Topics: Agaricales; Animals; Cell Shape; Melanins; Melanoma, Experimental; Mice; Microphthalmia-Associated T

2019
Evaluation of the Novel Synthetic Tyrosinase Inhibitor (
    Molecules (Basel, Switzerland), 2018, Dec-13, Volume: 23, Issue:12

    Topics: Agaricales; Animals; Cell Survival; Chromans; Computer Simulation; Drug Design; Enzyme Inhibitors; I

2018
Novel virtual screening approach for the discovery of human tyrosinase inhibitors.
    PloS one, 2014, Volume: 9, Issue:11

    Topics: Agaricales; Algorithms; Animals; Cell Line, Tumor; Drug Discovery; Enzyme Inhibitors; Fungal Protein

2014
Inhibition of melanogenesis by 2-[4-(5-chlorobenzo[d]thiazol-2-yl)phenoxy]-2-methylpropanoic acid (MHY908).
    Archives of pharmacal research, 2015, Volume: 38, Issue:4

    Topics: Agaricales; Animals; Cell Survival; Dose-Response Relationship, Drug; Enzyme Inhibitors; Melanins; M

2015
Design, synthesis, and anti-melanogenic effects of (E)-2-benzoyl-3-(substituted phenyl)acrylonitriles.
    Drug design, development and therapy, 2015, Volume: 9

    Topics: Acrylonitrile; Agaricales; Animals; Binding Sites; Cell Line, Tumor; Dose-Response Relationship, Dru

2015
Populus nigra (Salicaceae) absolute rich in phenolic acids, phenylpropanoïds and flavonoids as a new potent tyrosinase inhibitor.
    Fitoterapia, 2016, Volume: 111

    Topics: Agaricales; Animals; Flavonoids; Humans; Hydroxybenzoates; Melanins; Melanocytes; Melanoma, Experime

2016
Novel synthetic kojic acid-methimazole derivatives inhibit mushroom tyrosinase and melanogenesis.
    Journal of bioscience and bioengineering, 2016, Volume: 122, Issue:6

    Topics: Agaricales; Animals; Biphenyl Compounds; Chick Embryo; Enzyme Inhibitors; Melanins; Melanoma, Experi

2016
Simultaneous delivery of Paclitaxel and Bcl-2 siRNA via pH-Sensitive liposomal nanocarrier for the synergistic treatment of melanoma.
    Scientific reports, 2016, 10-27, Volume: 6

    Topics: Animals; Antineoplastic Agents, Phytogenic; Apoptosis; Cell Line, Tumor; Drug Compounding; Drug Deli

2016
Biodegradable Kojic Acid-Based Polymers: Controlled Delivery of Bioactives for Melanogenesis Inhibition.
    Biomacromolecules, 2017, 02-13, Volume: 18, Issue:2

    Topics: Animals; Biocompatible Materials; Cell Survival; Drug Delivery Systems; Melanins; Melanoma, Experime

2017
1-(2,4-dihydroxyphenyl)-3-(2,4-dimethoxy-3-methylphenyl)propane, a novel tyrosinase inhibitor with strong depigmenting effects.
    Chemical & pharmaceutical bulletin, 2008, Volume: 56, Issue:9

    Topics: Agaricales; Animals; Antioxidants; Cell Line; Dermatologic Agents; Enzyme Inhibitors; Kinetics; Lili

2008
Inhibitory effect of Cucumis sativus on melanin production in melanoma B16 cells by downregulation of tyrosinase expression.
    Planta medica, 2008, Volume: 74, Issue:15

    Topics: Animals; Antioxidants; Cucumis sativus; Hyperpigmentation; Melanins; Melanoma, Experimental; Mice; M

2008
Inhibitory effect of 2,4,2',4'-tetrahydroxy-3-(3-methyl-2-butenyl)-chalcone on tyrosinase activity and melanin biosynthesis.
    Biological & pharmaceutical bulletin, 2009, Volume: 32, Issue:1

    Topics: alpha-MSH; Animals; Antioxidants; Cell Line, Tumor; Cell Survival; Chalcone; Dopamine Agents; Dose-R

2009
p-coumaric acid not only inhibits human tyrosinase activity in vitro but also melanogenesis in cells exposed to UVB.
    Phytotherapy research : PTR, 2010, Volume: 24, Issue:8

    Topics: Agaricales; Animals; Arbutin; Cells, Cultured; Coumaric Acids; Dihydroxyphenylalanine; Epidermal Cel

2010
Inhibitory effects of 2-amino-3H-phenoxazin-3-one on the melanogenesis of murine B16 melanoma cell line.
    Bioscience, biotechnology, and biochemistry, 2010, Volume: 74, Issue:4

    Topics: Agaricales; Animals; Cell Line, Tumor; Indoles; Melanins; Melanoma; Melanoma, Experimental; Mice; Mi

2010
Dimeric cinnamoylamide derivatives as inhibitors of melanogenesis.
    Biological & pharmaceutical bulletin, 2011, Volume: 34, Issue:3

    Topics: Animals; Cell Line; Cell Line, Tumor; Coumaric Acids; Dermatologic Agents; Dimerization; Ethylenedia

2011
Cellular fusion and whitening effect of a chitosan derivative coated liposome.
    Colloids and surfaces. B, Biointerfaces, 2012, Feb-01, Volume: 90

    Topics: Animals; Antioxidants; Cell Fusion; Cell Line, Tumor; Cell Proliferation; Chitin; Cholesterol; Fibro

2012
Effects of ortho-dihydroxyisoflavone derivatives from Korean fermented soybean paste on melanogenesis in B16 melanoma cells and human skin equivalents.
    Phytotherapy research : PTR, 2012, Volume: 26, Issue:8

    Topics: Animals; Antineoplastic Agents, Phytogenic; Cell Proliferation; Cell Survival; Enzyme Activation; Fe

2012
Depigmenting effect of Kojic acid esters in hyperpigmented B16F1 melanoma cells.
    Journal of biomedicine & biotechnology, 2012, Volume: 2012

    Topics: Animals; Cell Line, Tumor; Dose-Response Relationship, Drug; Esters; Melanins; Melanoma, Experimenta

2012
Design, synthesis, and evaluation of (E)-N-substituted benzylidene-aniline derivatives as tyrosinase inhibitors.
    European journal of medicinal chemistry, 2012, Volume: 57

    Topics: Agaricales; alpha-MSH; Aniline Compounds; Animals; Antineoplastic Agents; Benzylidene Compounds; Cat

2012
A novel synthesized tyrosinase inhibitor: (E)-2-((2,4-dihydroxyphenyl)diazenyl)phenyl 4-methylbenzenesulfonate as an azo-resveratrol analog.
    Bioscience, biotechnology, and biochemistry, 2013, Volume: 77, Issue:1

    Topics: Animals; Azo Compounds; Benzenesulfonates; Cell Line, Tumor; Cell Survival; Dose-Response Relationsh

2013
Gnetol as a potent tyrosinase inhibitor from genus Gnetum.
    Bioscience, biotechnology, and biochemistry, 2003, Volume: 67, Issue:3

    Topics: Animals; Gnetum; Inhibitory Concentration 50; Melanins; Melanoma, Experimental; Mice; Peptides; Pyro

2003
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; Hydroquinon

2007
Piceatannol inhibits melanogenesis by its antioxidative actions.
    Biological & pharmaceutical bulletin, 2007, Volume: 30, Issue:11

    Topics: Animals; Antioxidants; Cell Line, Tumor; Dose-Response Relationship, Drug; Down-Regulation; Glutathi

2007
Glycine inhibits melanogenesis in vitro and causes hypopigmentation in vivo.
    Biological & pharmaceutical bulletin, 2007, Volume: 30, Issue:11

    Topics: alpha-MSH; Amino Acids; Animals; Antioxidants; Cell Line, Tumor; Dose-Response Relationship, Drug; F

2007
Oxyresveratrol and hydroxystilbene compounds. Inhibitory effect on tyrosinase and mechanism of action.
    The Journal of biological chemistry, 2002, May-03, Volume: 277, Issue:18

    Topics: Agaricales; Animals; Antioxidants; Enzyme Inhibitors; Gene Expression Regulation, Enzymologic; Kinet

2002