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Journal Abstract Search

374 related items for PubMed ID: 34070680

  • 1. Urolithin and Reduced Urolithin Derivatives as Potent Inhibitors of Tyrosinase and Melanogenesis: Importance of the 4-Substituted Resorcinol Moiety.
    Lee S, Choi H, Park Y, Jung HJ, Ullah S, Choi I, Kang D, Park C, Ryu IY, Jeong Y, Hwang Y, Hong S, Chun P, Moon HR.
    Int J Mol Sci; 2021 May 25; 22(11):. PubMed ID: 34070680
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  • 3. Novel Anti-Melanogenic Compounds, (Z)-5-(Substituted Benzylidene)-4-thioxothiazolidin-2-one Derivatives: In Vitro and In Silico Insights.
    Choi H, Ryu IY, Choi I, Ullah S, Jung HJ, Park Y, Jeong Y, Hwang Y, Hong S, Yoon IS, Yun H, Kim MS, Yoo JW, Jung Y, Chun P, Moon HR.
    Molecules; 2021 Aug 17; 26(16):. PubMed ID: 34443550
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  • 4. (E)-2-Cyano-3-(substituted phenyl)acrylamide analogs as potent inhibitors of tyrosinase: A linear β-phenyl-α,β-unsaturated carbonyl scaffold.
    Son S, Kim H, Yun HY, Kim DH, Ullah S, Kim SJ, Kim YJ, Kim MS, Yoo JW, Chun P, Moon HR.
    Bioorg Med Chem; 2015 Dec 15; 23(24):7728-34. PubMed ID: 26631438
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  • 11. Antioxidant, anti-tyrosinase and anti-melanogenic effects of (E)-2,3-diphenylacrylic acid derivatives.
    Ullah S, Park Y, Park C, Lee S, Kang D, Yang J, Akter J, Chun P, Moon HR.
    Bioorg Med Chem; 2019 Jun 01; 27(11):2192-2200. PubMed ID: 31027707
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  • 12. 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 01; 49():245-52. PubMed ID: 22301213
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  • 13. Thiazol-4(5H)-one analogs as potent tyrosinase inhibitors: Synthesis, tyrosinase inhibition, antimelanogenic effect, antioxidant activity, and in silico docking simulation.
    Jung Park Y, Jin Jung H, Jin Kim H, Soo Park H, Lee J, Yoon D, Kyung Kang M, Young Kim G, Ullah S, Kang D, Park Y, Chun P, Young Chung H, Ryong Moon H.
    Bioorg Med Chem; 2024 Jan 15; 98():117578. PubMed ID: 38154348
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  • 15. In vitro anti-melanogenic effects of chimeric compounds, 2-(substituted benzylidene)-1,3-indanedione derivatives with a β-phenyl-α, β -unsaturated dicarbonyl scaffold.
    Ryu IY, Choi I, Jung HJ, Ullah S, Choi H, Al-Amin M, Chun P, Moon HR.
    Bioorg Chem; 2021 Apr 15; 109():104688. PubMed ID: 33582586
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  • 16. Tyrosinase inhibition and anti-melanin generation effect of cinnamamide analogues.
    Ullah S, Park C, Ikram M, Kang D, Lee S, Yang J, Park Y, Yoon S, Chun P, Moon HR.
    Bioorg Chem; 2019 Jun 15; 87():43-55. PubMed ID: 30856375
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  • 17. (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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  • 19. Synthesis and biological activity of hydroxy substituted phenyl-benzo[d]thiazole analogues for antityrosinase activity in B16 cells.
    Ha YM, Park JY, Park YJ, Park D, Choi YJ, Kim JM, Lee EK, Han YK, Kim JA, Lee JY, Moon HR, Chung HY.
    Bioorg Med Chem Lett; 2011 Apr 15; 21(8):2445-9. PubMed ID: 21397499
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  • 20. Anti-tyrosinase flavone derivatives and their anti-melanogenic activities: Importance of the β-phenyl-α,β-unsaturated carbonyl scaffold.
    Lee J, Jeong Y, Jin Jung H, Ullah S, Ko J, Young Kim G, Yoon D, Hong S, Kang D, Park Y, Chun P, Young Chung H, Ryong Moon H.
    Bioorg Chem; 2023 Jun 15; 135():106504. PubMed ID: 37015153
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