313 related articles for article (PubMed ID: 30130649)
21. 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]
22. Flavones as tyrosinase inhibitors: kinetic studies in vitro and in silico.
Arroo RRJ; Sari S; Barut B; Özel A; Ruparelia KC; Şöhretoğlu D
Phytochem Anal; 2020 May; 31(3):314-321. PubMed ID: 31997462
[TBL] [Abstract][Full Text] [Related]
23. Kojic acid-amino acid conjugates as tyrosinase inhibitors.
Noh JM; Kwak SY; Seo HS; Seo JH; Kim BG; Lee YS
Bioorg Med Chem Lett; 2009 Oct; 19(19):5586-9. PubMed ID: 19700313
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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; 13(5):531-8. PubMed ID: 27061023
[TBL] [Abstract][Full Text] [Related]
26. 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; 90(5):804-810. PubMed ID: 28390091
[TBL] [Abstract][Full Text] [Related]
27. Structure-based modification of 3-/4-aminoacetophenones giving a profound change of activity on tyrosinase: from potent activators to highly efficient inhibitors.
You A; Zhou J; Song S; Zhu G; Song H; Yi W
Eur J Med Chem; 2015 Mar; 93():255-62. PubMed ID: 25686594
[TBL] [Abstract][Full Text] [Related]
28. Molecular docking studies and biological evaluation of 1,3,4-thiadiazole derivatives bearing Schiff base moieties as tyrosinase inhibitors.
Tang J; Liu J; Wu F
Bioorg Chem; 2016 Dec; 69():29-36. PubMed ID: 27669118
[TBL] [Abstract][Full Text] [Related]
29. Phosphonic and Phosphinic Acid Derivatives as Novel Tyrosinase Inhibitors: Kinetic Studies and Molecular Docking.
Wolińska E; Hałdys K; Góra J; Olszewski TK; Boduszek B; Latajka R
Chem Biodivers; 2019 Jul; 16(7):e1900167. PubMed ID: 31145516
[TBL] [Abstract][Full Text] [Related]
30. Inhibitory effect of morin on tyrosinase: insights from spectroscopic and molecular docking studies.
Wang Y; Zhang G; Yan J; Gong D
Food Chem; 2014 Nov; 163():226-33. PubMed ID: 24912720
[TBL] [Abstract][Full Text] [Related]
31. Highly potent tyrosinase inhibitor, neorauflavane from Campylotropis hirtella and inhibitory mechanism with molecular docking.
Tan X; Song YH; Park C; Lee KW; Kim JY; Kim DW; Kim KD; Lee KW; Curtis-Long MJ; Park KH
Bioorg Med Chem; 2016 Jan; 24(2):153-9. PubMed ID: 26706112
[TBL] [Abstract][Full Text] [Related]
32. Prenylated flavonoids as tyrosinase inhibitors.
Lee NK; Son KH; Chang HW; Kang SS; Park H; Heo MY; Kim HP
Arch Pharm Res; 2004 Nov; 27(11):1132-5. PubMed ID: 15595416
[TBL] [Abstract][Full Text] [Related]
33. Flavonoids as mushroom tyrosinase inhibitors: a fluorescence quenching study.
Kim D; Park J; Kim J; Han C; Yoon J; Kim N; Seo J; Lee C
J Agric Food Chem; 2006 Feb; 54(3):935-41. PubMed ID: 16448205
[TBL] [Abstract][Full Text] [Related]
34. 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
[TBL] [Abstract][Full Text] [Related]
35. Novel morpholine containing cinnamoyl amides as potent tyrosinase inhibitors.
Ghafary S; Ranjbar S; Larijani B; Amini M; Biglar M; Mahdavi M; Bakhshaei M; Khoshneviszadeh M; Sakhteman A; Khoshneviszadeh M
Int J Biol Macromol; 2019 Aug; 135():978-985. PubMed ID: 31150673
[TBL] [Abstract][Full Text] [Related]
36. 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
[TBL] [Abstract][Full Text] [Related]
37. Functionality study of chalcone-hydroxypyridinone hybrids as tyrosinase inhibitors and influence on anti-tyrosinase activity.
Singh LR; Chen YL; Xie YY; Xia W; Gong XW; Hider RC; Zhou T
J Enzyme Inhib Med Chem; 2020 Dec; 35(1):1562-1567. PubMed ID: 32746652
[TBL] [Abstract][Full Text] [Related]
38. Study on Synthesis and Biological Evaluation of 3-Aryl Substituted Xanthone Derivatives as Novel and Potent Tyrosinase Inhibitors.
Yu L; Chen L; Luo G; Liu L; Zhu W; Yan P; Zhang P; Zhang C; Wu W
Chem Pharm Bull (Tokyo); 2019 Nov; 67(11):1232-1241. PubMed ID: 31495804
[TBL] [Abstract][Full Text] [Related]
39. Synthesis of aryl pyrazole via Suzuki coupling reaction, in vitro mushroom tyrosinase enzyme inhibition assay and in silico comparative molecular docking analysis with Kojic acid.
Channar PA; Saeed A; Larik FA; Batool B; Kalsoom S; Hasan MM; Erben MF; El-Seedi HR; Ali M; Ashraf Z
Bioorg Chem; 2018 Sep; 79():293-300. PubMed ID: 29793142
[TBL] [Abstract][Full Text] [Related]
40. Design, synthesis, and antimelanogenic effects of (2-substituted phenyl-1,3-dithiolan-4-yl)methanol derivatives.
Kim DH; Kim SJ; Ullah S; Yun HY; Chun P; Moon HR
Drug Des Devel Ther; 2017; 11():827-836. PubMed ID: 28352157
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]