BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

277 related articles for article (PubMed ID: 28867710)

  • 1. Design, Synthesis and Biological Evaluation of Oxindole-Based Chalcones as Small-Molecule Inhibitors of Melanogenic Tyrosinase.
    Suthar SK; Bansal S; Narkhede N; Guleria M; Alex AT; Joseph A
    Chem Pharm Bull (Tokyo); 2017; 65(9):833-839. PubMed ID: 28867710
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Integrated kinetic studies and computational analysis on naphthyl chalcones as mushroom tyrosinase inhibitors.
    Radhakrishnan S; Shimmon R; Conn C; Baker A
    Bioorg Med Chem Lett; 2015 Oct; 25(19):4085-91. PubMed ID: 26318997
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Microwave-assisted synthesis and tyrosinase inhibitory activity of chalcone derivatives.
    Liu J; Chen C; Wu F; Zhao L
    Chem Biol Drug Des; 2013 Jul; 82(1):39-47. PubMed ID: 23461881
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Structure-Based Design, Synthesis, Biological Evaluation and Molecular Docking Study of 4-Hydroxy-N'-methylenebenzohydrazide Derivatives Acting as Tyrosinase Inhibitors with Potentiate Anti-Melanogenesis Activities.
    Iraji A; Khoshneviszadeh M; Bakhshizadeh P; Edraki N; Khoshneviszadeh M
    Med Chem; 2020; 16(7):892-902. PubMed ID: 31339074
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inhibition of tyrosinase activity and melanin production by the chalcone derivative 1-(2-cyclohexylmethoxy-6-hydroxy-phenyl)-3-(4-hydroxymethyl-phenyl)-propenone.
    Kim BH; Park KC; Park JH; Lee CG; Ye SK; Park JY
    Biochem Biophys Res Commun; 2016 Nov; 480(4):648-654. PubMed ID: 27983977
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evaluation of Novel Chalcone Oximes as Inhibitors of Tyrosinase and Melanin Formation in B16 Cells.
    Radhakrishnan SK; Shimmon RG; Conn C; Baker AT
    Arch Pharm (Weinheim); 2016 Jan; 349(1):20-9. PubMed ID: 26575580
    [TBL] [Abstract][Full Text] [Related]  

  • 7. (
    Jung HJ; Noh SG; Ryu IY; Park C; Lee JY; Chun P; Moon HR; Chung HY
    Molecules; 2020 Nov; 25(22):. PubMed ID: 33233397
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Design, synthesis and biological evaluation of hydroxy substituted amino chalcone compounds for antityrosinase activity in B16 cells.
    Radhakrishnan S; Shimmon R; Conn C; Baker A
    Bioorg Chem; 2015 Oct; 62():117-23. PubMed ID: 26333206
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Design, synthesis, and anti-melanogenic effects of (E)-2-benzoyl-3-(substituted phenyl)acrylonitriles.
    Yun HY; Kim DH; Son S; Ullah S; Kim SJ; Kim YJ; Yoo JW; Jung Y; Chun P; Moon HR
    Drug Des Devel Ther; 2015; 9():4259-68. PubMed ID: 26347064
    [TBL] [Abstract][Full Text] [Related]  

  • 10. New tyrosinase inhibitory decapeptide: Molecular insights into the role of tyrosine residues.
    Ochiai A; Tanaka S; Imai Y; Yoshida H; Kanaoka T; Tanaka T; Taniguchi M
    J Biosci Bioeng; 2016 Jun; 121(6):607-613. PubMed ID: 26589783
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Azachalcones: a new class of potent polyphenol oxidase inhibitors.
    Radhakrishnan SK; Shimmon RG; Conn C; Baker AT
    Bioorg Med Chem Lett; 2015 Apr; 25(8):1753-1756. PubMed ID: 25782744
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel bioactive chalcone of Morus australis inhibits tyrosinase activity and melanin biosynthesis in B16 melanoma cells.
    Takahashi M; Takara K; Toyozato T; Wada K
    J Oleo Sci; 2012; 61(10):585-92. PubMed ID: 23018855
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Functionality study of chalcone-hydroxypyridinone hybrids as tyrosinase inhibitors and influence on anti-tyrosinase activity.
    Singh LR; Chen YL; Xie YY; Xia W; Gong XW; Hider RC; Zhou T
    J Enzyme Inhib Med Chem; 2020 Dec; 35(1):1562-1567. PubMed ID: 32746652
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesis and evaluation of 2',4',6'-trihydroxychalcones as a new class of tyrosinase inhibitors.
    Jun N; Hong G; Jun K
    Bioorg Med Chem; 2007 Mar; 15(6):2396-402. PubMed ID: 17267225
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identifying melanogenesis inhibitors from Cinnamomum subavenium with in vitro and in vivo screening systems by targeting the human tyrosinase.
    Wang HM; Chen CY; Wen ZH
    Exp Dermatol; 2011 Mar; 20(3):242-8. PubMed ID: 21054558
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Structural requirement of phenylthiourea analogs for their inhibitory activity of melanogenesis and tyrosinase.
    Thanigaimalai P; Lee KC; Sharma VK; Joo C; Cho WJ; Roh E; Kim Y; Jung SH
    Bioorg Med Chem Lett; 2011 Nov; 21(22):6824-8. PubMed ID: 21978680
    [TBL] [Abstract][Full Text] [Related]  

  • 17. In vitro and in vivo evidence of tyrosinase inhibitory activity of a synthesized (Z)-5-(3-hydroxy-4-methoxybenzylidene)-2-thioxothiazolidin-4-one (5-HMT).
    Bang E; Lee EK; Noh SG; Jung HJ; Moon KM; Park MH; Park YJ; Hyun MK; Lee AK; Kim SJ; Yang J; Park Y; Chun P; Moon HR; Chung HY
    Exp Dermatol; 2019 Jun; 28(6):734-737. PubMed ID: 30554432
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phloretin as both a substrate and inhibitor of tyrosinase: Inhibitory activity and mechanism.
    Chen J; Li Q; Ye Y; Huang Z; Ruan Z; Jin N
    Spectrochim Acta A Mol Biomol Spectrosc; 2020 Feb; 226():117642. PubMed ID: 31614273
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Reversible and competitive inhibitory kinetics of amoxicillin on mushroom tyrosinase.
    Chen XX; Zhang J; Chai WM; Feng HL; Xiang ZH; Shen DY; Chen QX
    Int J Biol Macromol; 2013 Nov; 62():726-33. PubMed ID: 24099941
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Highly potent tyrosinase inhibitor, neorauflavane from Campylotropis hirtella and inhibitory mechanism with molecular docking.
    Tan X; Song YH; Park C; Lee KW; Kim JY; Kim DW; Kim KD; Lee KW; Curtis-Long MJ; Park KH
    Bioorg Med Chem; 2016 Jan; 24(2):153-9. PubMed ID: 26706112
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.