BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

392 related articles for article (PubMed ID: 17267225)

  • 1. 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]  

  • 2. 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]  

  • 3. Synthesis and evaluation of 5-benzylidene(thio)barbiturate-beta-D-glycosides as mushroom tyrosinase inhibitors.
    Yan Q; Cao R; Yi W; Yu L; Chen Z; Ma L; Song H
    Bioorg Med Chem Lett; 2009 Aug; 19(15):4055-8. PubMed ID: 19564107
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chalcones as potent tyrosinase inhibitors: the importance of a 2,4-substituted resorcinol moiety.
    Khatib S; Nerya O; Musa R; Shmuel M; Tamir S; Vaya J
    Bioorg Med Chem; 2005 Jan; 13(2):433-41. PubMed ID: 15598564
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis and biological evaluation of polyhydroxy benzophenone as mushroom tyrosinase inhibitors.
    Wu J; Hu X; Ma L
    J Enzyme Inhib Med Chem; 2011 Jun; 26(3):449-52. PubMed ID: 20939763
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis and biological evaluation of novel 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors.
    Yi W; Cao R; Peng W; Wen H; Yan Q; Zhou B; Ma L; Song H
    Eur J Med Chem; 2010 Feb; 45(2):639-46. PubMed ID: 19932528
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds.
    Liu J; Cao R; Yi W; Ma C; Wan Y; Zhou B; Ma L; Song H
    Eur J Med Chem; 2009 Apr; 44(4):1773-8. PubMed ID: 18524420
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Synthesis and biological evaluation of helicid analogues as mushroom tyrosinase inhibitors.
    Yi W; Cao R; Wen H; Yan Q; Zhou B; Wan Y; Ma L; Song H
    Bioorg Med Chem Lett; 2008 Dec; 18(24):6490-3. PubMed ID: 18996693
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Design and synthesis of 5-(substituted benzylidene)thiazolidine-2,4-dione derivatives as novel tyrosinase inhibitors.
    Ha YM; Park YJ; Kim JA; Park D; Park JY; Lee HJ; Lee JY; Moon HR; Chung HY
    Eur J Med Chem; 2012 Mar; 49():245-52. PubMed ID: 22301213
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chalcones as potent tyrosinase inhibitors: the effect of hydroxyl positions and numbers.
    Nerya O; Musa R; Khatib S; Tamir S; Vaya J
    Phytochemistry; 2004 May; 65(10):1389-95. PubMed ID: 15231412
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evaluation of dihydropyrimidin-(2H)-one analogues and rhodanine derivatives as tyrosinase inhibitors.
    Liu J; Wu F; Chen L; Hu J; Zhao L; Chen C; Peng L
    Bioorg Med Chem Lett; 2011 Apr; 21(8):2376-9. PubMed ID: 21411319
    [TBL] [Abstract][Full Text] [Related]  

  • 13. TOMOCOMD-CARDD descriptors-based virtual screening of tyrosinase inhibitors: evaluation of different classification model combinations using bond-based linear indices.
    Casañola-Martín GM; Marrero-Ponce Y; Khan MT; Ather A; Sultan S; Torrens F; Rotondo R
    Bioorg Med Chem; 2007 Feb; 15(3):1483-503. PubMed ID: 17110117
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Design, synthesis and biological evaluation of hydroxy- or methoxy-substituted 5-benzylidene(thio) barbiturates as novel tyrosinase inhibitors.
    Chen Z; Cai D; Mou D; Yan Q; Sun Y; Pan W; Wan Y; Song H; Yi W
    Bioorg Med Chem; 2014 Jul; 22(13):3279-84. PubMed ID: 24857777
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Discovery of 4-functionalized phenyl-O-beta-D-glycosides as a new class of mushroom tyrosinase inhibitors.
    Yi W; Cao R; Wen H; Yan Q; Zhou B; Ma L; Song H
    Bioorg Med Chem Lett; 2009 Nov; 19(21):6157-60. PubMed ID: 19800229
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Design and synthesis of 3,5-diaryl-4,5-dihydro-1H-pyrazoles as new tyrosinase inhibitors.
    Zhou Z; Zhuo J; Yan S; Ma L
    Bioorg Med Chem; 2013 Apr; 21(7):2156-62. PubMed ID: 23391365
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Design and synthesis of biphenyl derivatives as mushroom tyrosinase inhibitors.
    Bao K; Dai Y; Zhu ZB; Tu FJ; Zhang WG; Yao XS
    Bioorg Med Chem; 2010 Sep; 18(18):6708-14. PubMed ID: 20729091
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New halogenated phenylcoumarins as tyrosinase inhibitors.
    Matos MJ; Santana L; Uriarte E; Delogu G; Corda M; Fadda MB; Era B; Fais A
    Bioorg Med Chem Lett; 2011 Jun; 21(11):3342-5. PubMed ID: 21514152
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synthesis and tyrosinase inhibitory activity of novel N-hydroxybenzyl-N-nitrosohydroxylamines.
    Shiino M; Watanabe Y; Umezawa K
    Bioorg Chem; 2003 Apr; 31(2):129-35. PubMed ID: 12729570
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.