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Journal Abstract Search

236 related items for PubMed ID: 31518762

  • 1. Tyrosinase inhibitory effects of Vinca major and its secondary metabolites: Enzyme kinetics and in silico inhibition model of the metabolites validated by pharmacophore modelling.
    Sari S, Barut B, Özel A, Şöhretoğlu D.
    Bioorg Chem; 2019 Nov; 92():103259. PubMed ID: 31518762
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  • 4. Tyrosinase and α-glucosidase inhibitory potential of compounds isolated from Quercus coccifera bark: In vitro and in silico perspectives.
    Sari S, Barut B, Özel A, Kuruüzüm-Uz A, Şöhretoğlu D.
    Bioorg Chem; 2019 May; 86():296-304. PubMed ID: 30738329
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  • 7. 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
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  • 8. 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 01; 30(6):874-83. PubMed ID: 25643758
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  • 9. 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 01; 108():205-213. PubMed ID: 29180052
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  • 10. (E)-1-(Furan-2-yl)-(substituted phenyl)prop-2-en-1-one Derivatives as Tyrosinase Inhibitors and Melanogenesis Inhibition: An In Vitro and In Silico Study.
    Jung HJ, Noh SG, Ryu IY, Park C, Lee JY, Chun P, Moon HR, Chung HY.
    Molecules; 2020 Nov 21; 25(22):. PubMed ID: 33233397
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  • 13. Tyrosinase inhibition by some flavonoids: Inhibitory activity, mechanism by in vitro and in silico studies.
    Şöhretoğlu D, Sari S, Barut B, Özel A.
    Bioorg Chem; 2018 Dec 21; 81():168-174. PubMed ID: 30130649
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  • 14. Design and synthesis of novel hydroxypyridinone derivatives as potential tyrosinase inhibitors.
    Zhao DY, Zhang MX, Dong XW, Hu YZ, Dai XY, Wei X, Hider RC, Zhang JC, Zhou T.
    Bioorg Med Chem Lett; 2016 Jul 01; 26(13):3103-3108. PubMed ID: 27185329
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  • 15. Inhibition of tyrosinase by 4H-chromene analogs: Synthesis, kinetic studies, and computational analysis.
    Brasil EM, Canavieira LM, Cardoso ÉTC, Silva EO, Lameira J, Nascimento JLM, Eifler-Lima VL, Macchi BM, Sriram D, Bernhardt PV, Silva JRA, Williams CM, Alves CN.
    Chem Biol Drug Des; 2017 Nov 01; 90(5):804-810. PubMed ID: 28390091
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  • 16. 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 Nov 01; 15(7):715-728. PubMed ID: 30892163
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  • 17. 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
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  • 18. 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 01; 22(13):3279-84. PubMed ID: 24857777
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