These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 20359890)

  • 1. Structural requirement(s) of N-phenylthioureas and benzaldehyde thiosemicarbazones as inhibitors of melanogenesis in melanoma B 16 cells.
    Thanigaimalai P; Hoang TA; Lee KC; Bang SC; Sharma VK; Yun CY; Roh E; Hwang BY; Kim Y; Jung SH
    Bioorg Med Chem Lett; 2010 May; 20(9):2991-3. PubMed ID: 20359890
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Structural characteristics of thiosemicarbazones as inhibitors of melanogenesis.
    Lee KC; Thanigaimalai P; Sharma VK; Kim MS; Roh E; Hwang BY; Kim Y; Jung SH
    Bioorg Med Chem Lett; 2010 Nov; 20(22):6794-6. PubMed ID: 20863702
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synthesis and antityrosinase mechanism of benzaldehyde thiosemicarbazones: novel tyrosinase inhibitors.
    Chen LH; Hu YH; Song W; Song KK; Liu X; Jia YL; Zhuang JX; Chen QX
    J Agric Food Chem; 2012 Feb; 60(6):1542-7. PubMed ID: 22250887
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ketonethiosemicarbazones: structure-activity relationships for their melanogenesis inhibition.
    Thanigaimalai P; Lee KC; Sharma VK; Roh E; Kim Y; Jung SH
    Bioorg Med Chem Lett; 2011 Jun; 21(12):3527-30. PubMed ID: 21601449
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analogues of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea as inhibitors of tyrosinase and melanin formation.
    Criton M; Le Mellay-Hamon V
    Bioorg Med Chem Lett; 2008 Jun; 18(12):3607-10. PubMed ID: 18501598
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Melanogenesis inhibitors from the rhizomes of Alpinia officinarum in B16 melanoma cells.
    Matsuda H; Nakashima S; Oda Y; Nakamura S; Yoshikawa M
    Bioorg Med Chem; 2009 Aug; 17(16):6048-53. PubMed ID: 19615910
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis and biological evaluation of phenolic Mannich bases of benzaldehyde and (thio)semicarbazone derivatives against the cysteine protease falcipain-2 and a chloroquine resistant strain of Plasmodium falciparum.
    Chipeleme A; Gut J; Rosenthal PJ; Chibale K
    Bioorg Med Chem; 2007 Jan; 15(1):273-82. PubMed ID: 17052908
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 3D-QSAR and molecular docking studies of benzaldehyde thiosemicarbazone, benzaldehyde, benzoic acid, and their derivatives as phenoloxidase inhibitors.
    Xue CB; Zhang L; Luo WC; Xie XY; Jiang L; Xiao T
    Bioorg Med Chem; 2007 Mar; 15(5):2006-15. PubMed ID: 17258462
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exploring the interaction of N/S compounds with a dicopper center: tyrosinase inhibition and model studies.
    Buitrago E; Vuillamy A; Boumendjel A; Yi W; Gellon G; Hardré R; Philouze C; Serratrice G; Jamet H; Réglier M; Belle C
    Inorg Chem; 2014 Dec; 53(24):12848-58. PubMed ID: 25415587
    [TBL] [Abstract][Full Text] [Related]  

  • 11. QSAR and kinetics of the inhibition of benzaldehyde derivatives against Sacrophaga neobelliaria phenoloxidase.
    Li W; Kubo I
    Bioorg Med Chem; 2004 Feb; 12(4):701-13. PubMed ID: 14759731
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The phenylthiourea is a competitive inhibitor of the enzymatic oxidation of DOPA by phenoloxidase.
    Ryazanova AD; Alekseev AA; Slepneva IA
    J Enzyme Inhib Med Chem; 2012 Feb; 27(1):78-83. PubMed ID: 21534859
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inhibition of xanthine oxidase by thiosemicarbazones, hydrazones and dithiocarbazates derived from hydroxy-substituted benzaldehydes.
    Leigh M; Raines DJ; Castillo CE; Duhme-Klair AK
    ChemMedChem; 2011 Jun; 6(6):1107-18. PubMed ID: 21480532
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Antityrosinase and antimicrobial activities of trans-cinnamaldehyde thiosemicarbazone.
    Zhu YJ; Song KK; Li ZC; Pan ZZ; Guo YJ; Zhou JJ; Wang Q; Liu B; Chen QX
    J Agric Food Chem; 2009 Jun; 57(12):5518-23. PubMed ID: 19462982
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Procyanidin trimers to pentamers fractionated from apple inhibit melanogenesis in B16 mouse melanoma cells.
    Shoji T; Masumoto S; Moriichi N; Kobori M; Kanda T; Shinmoto H; Tsushida T
    J Agric Food Chem; 2005 Jul; 53(15):6105-11. PubMed ID: 16029003
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 4-methyl-5-amino-1-formylisoquinoline thiosemicarbazone, a second-generation antineoplastic agent of the alpha-(N)-heterocyclic carboxaldehyde thiosemicarbazone series.
    Agrawal KC; Schenkman JB; Denk H; Mooney PD; Moore EC; Wodinsky I; Sartorelli AC
    Cancer Res; 1977 Jun; 37(6):1692-6. PubMed ID: 870183
    [TBL] [Abstract][Full Text] [Related]  

  • 17. N-[(Dihydroxyphenyl)acyl]serotonins as potent inhibitors of tyrosinase from mouse and human melanoma cells.
    Yamazaki Y; Kawano Y; Yamanaka A; Maruyama S
    Bioorg Med Chem Lett; 2009 Aug; 19(15):4178-82. PubMed ID: 19524439
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Study on the design, synthesis and structure-activity relationships of new thiosemicarbazone compounds as tyrosinase inhibitors.
    Song S; You A; Chen Z; Zhu G; Wen H; Song H; Yi W
    Eur J Med Chem; 2017 Oct; 139():815-825. PubMed ID: 28865277
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inhibitory effects of 6-(3-hydroxyphenyl)-2-naphthol on tyrosinase activity and melanin synthesis.
    Chung SW; Ha YM; Kim YJ; Song S; Lee H; Suh H; Chung HY
    Arch Pharm Res; 2009 Feb; 32(2):289-94. PubMed ID: 19280161
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Flavokawains B and C, melanogenesis inhibitors, isolated from the root of Piper methysticum and synthesis of analogs.
    Jeong HJ; Lee CS; Choi J; Hong YD; Shin SS; Park JS; Lee JH; Lee S; Yoon KD; Ko J
    Bioorg Med Chem Lett; 2015 Feb; 25(4):799-802. PubMed ID: 25597012
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.