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Journal Abstract Search

311 related items for PubMed ID: 31371919

  • 1. Evaluation of novel pyrimidine derivatives as a new class of mushroom tyrosinase inhibitor.
    Mirmortazavi SS, Farvandi M, Ghafouri H, Mohammadi A, Shourian M.
    Drug Des Devel Ther; 2019; 13():2169-2178. PubMed ID: 31371919
    [Abstract] [Full Text] [Related]

  • 2. Evaluation of thiazolidinone derivatives as a new class of mushroom tyrosinase inhibitors.
    Rezaei M, Mohammadi HT, Mahdavi A, Shourian M, Ghafouri H.
    Int J Biol Macromol; 2018 Mar; 108():205-213. PubMed ID: 29180052
    [Abstract] [Full Text] [Related]

  • 3. Synthesis, computational molecular docking analysis and effectiveness on tyrosinase inhibition of kojic acid derivatives.
    Karakaya G, Türe A, Ercan A, Öncül S, Aytemir MD.
    Bioorg Chem; 2019 Jul; 88():102950. PubMed ID: 31075740
    [Abstract] [Full Text] [Related]

  • 4. Design, synthesis, kinetic mechanism and molecular docking studies of novel 1-pentanoyl-3-arylthioureas as inhibitors of mushroom tyrosinase and free radical scavengers.
    Larik FA, Saeed A, Channar PA, Muqadar U, Abbas Q, Hassan M, Seo SY, Bolte M.
    Eur J Med Chem; 2017 Dec 01; 141():273-281. PubMed ID: 29040952
    [Abstract] [Full Text] [Related]

  • 5. Synthesis and biological evaluation of novel hydroxybenzaldehyde-based kojic acid analogues as inhibitors of mushroom tyrosinase.
    Xie W, Zhang H, He J, Zhang J, Yu Q, Luo C, Li S.
    Bioorg Med Chem Lett; 2017 Feb 01; 27(3):530-532. PubMed ID: 28011217
    [Abstract] [Full Text] [Related]

  • 6. Synthesis, molecular docking studies of coumarinyl-pyrazolinyl substituted thiazoles as non-competitive inhibitors of mushroom tyrosinase.
    Saeed A, Mahesar PA, Channar PA, Abbas Q, Larik FA, Hassan M, Raza H, Seo SY.
    Bioorg Chem; 2017 Oct 01; 74():187-196. PubMed ID: 28837887
    [Abstract] [Full Text] [Related]

  • 7. Inhibitory Kinetics of Azachalcones and their Oximes on Mushroom Tyrosinase: A Facile Solid-state Synthesis.
    Radhakrishnan SK, Shimmon RG, Conn C, Baker AT.
    Chem Biodivers; 2016 May 01; 13(5):531-8. PubMed ID: 27061023
    [Abstract] [Full Text] [Related]

  • 8. Synthesis, computational studies and enzyme inhibitory kinetics of substituted methyl[2-(4-dimethylamino-benzylidene)-hydrazono)-4-oxo-thiazolidin-5-ylidene]acetates as mushroom tyrosinase inhibitors.
    Channar PA, Saeed A, Larik FA, Rafiq M, Ashraf Z, Jabeen F, Fattah TA.
    Bioorg Med Chem; 2017 Nov 01; 25(21):5929-5938. PubMed ID: 28988751
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 21(8):2376-9. PubMed ID: 21411319
    [Abstract] [Full Text] [Related]

  • 10. Inhibitory effects of 1,3-selenazol-4-one derivatives on mushroom tyrosinase.
    Koketsu M, Choi SY, Ishihara H, Lim BO, Kim H, Kim SY.
    Chem Pharm Bull (Tokyo); 2002 Dec 15; 50(12):1594-6. PubMed ID: 12499597
    [Abstract] [Full Text] [Related]

  • 11. Synthesis of novel azo-resveratrol, azo-oxyresveratrol and their derivatives as potent tyrosinase inhibitors.
    Song YM, Ha YM, Kim JA, Chung KW, Uehara Y, Lee KJ, Chun P, Byun Y, Chung HY, Moon HR.
    Bioorg Med Chem Lett; 2012 Dec 15; 22(24):7451-5. PubMed ID: 23142612
    [Abstract] [Full Text] [Related]

  • 12. Carvacrol derivatives as mushroom tyrosinase inhibitors; synthesis, kinetics mechanism and molecular docking studies.
    Ashraf Z, Rafiq M, Nadeem H, Hassan M, Afzal S, Waseem M, Afzal K, Latip J.
    PLoS One; 2017 Dec 15; 12(5):e0178069. PubMed ID: 28542395
    [Abstract] [Full Text] [Related]

  • 13. Potent inhibitory effects of N-aryl S-alkylthiocarbamate derivatives on the dopa oxidase activity of mushroom tyrosinase.
    Lee KH, Koketsu M, Choi SY, Lee KJ, Lee P, Ishihara H, Kim SY.
    Chem Pharm Bull (Tokyo); 2005 Jul 15; 53(7):747-9. PubMed ID: 15997128
    [Abstract] [Full Text] [Related]

  • 14. Design, synthesis and bioevaluation of novel umbelliferone analogues as potential mushroom tyrosinase inhibitors.
    Ashraf Z, Rafiq M, Seo SY, Babar MM, Zaidi NU.
    J Enzyme Inhib Med Chem; 2015 Dec 15; 30(6):874-83. PubMed ID: 25643758
    [Abstract] [Full Text] [Related]

  • 15. Synthesis and biological evaluation of kojic acid derivatives containing 1,2,4-triazole as potent tyrosinase inhibitors.
    Xie W, Zhang J, Ma X, Yang W, Zhou Y, Tang X, Zou Y, Li H, He J, Xie S, Zhao Y, Liu F.
    Chem Biol Drug Des; 2015 Nov 15; 86(5):1087-92. PubMed ID: 25916324
    [Abstract] [Full Text] [Related]

  • 16. The tyrosinase inhibitory effects of isoxazolone derivatives with a (Z)-β-phenyl-α, β-unsaturated carbonyl scaffold.
    Kim SJ, Yang J, Lee S, Park C, Kang D, Akter J, Ullah S, Kim YJ, Chun P, Moon HR.
    Bioorg Med Chem; 2018 Aug 07; 26(14):3882-3889. PubMed ID: 29907470
    [Abstract] [Full Text] [Related]

  • 17. Synthesis, molecular docking and kinetic studies of novel quinolinyl based acyl thioureas as mushroom tyrosinase inhibitors and free radical scavengers.
    Mustafa MN, Saeed A, Channar PA, Larik FA, Zain-Ul Abideen M, Shabir G, Abbas Q, Hassan M, Raza H, Seo SY.
    Bioorg Chem; 2019 Sep 07; 90():103063. PubMed ID: 31220666
    [Abstract] [Full Text] [Related]

  • 18. Novel Amide Derivatives as Potent Tyrosinase Inhibitors; In-vitro, In-vivo Antimelanogenic Activity and Computational Studies.
    Ali A, Ashraf Z, Rafiq M, Kumar A, Jabeen F, Lee GJ, Nazir F, Ahmed M, Rhee M, Choi EH.
    Med Chem; 2019 Sep 07; 15(7):715-728. PubMed ID: 30892163
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 21(7):2156-62. PubMed ID: 23391365
    [Abstract] [Full Text] [Related]

  • 20. Inhibitory effects of N-(acryloyl)benzamide derivatives on tyrosinase and melanogenesis.
    Lee S, Ullah S, Park C, Won Lee H, Kang D, Yang J, Akter J, Park Y, Chun P, Moon HR.
    Bioorg Med Chem; 2019 Sep 01; 27(17):3929-3937. PubMed ID: 31345746
    [Abstract] [Full Text] [Related]

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