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Items: 1 to 20 of 149

1.

Synthesis and structure-activity relationships and effects of phenylpropanoid amides of octopamine and dopamine on tyrosinase inhibition and antioxidation.

Wu Z, Zheng L, Li Y, Su F, Yue X, Tang W, Ma X, Nie J, Li H.

Food Chem. 2012 Sep 15;134(2):1128-31. doi: 10.1016/j.foodchem.2012.02.152. Epub 2012 Mar 3.

PMID:
23107737
2.

Synthesis and structure-activity relationships of phenylpropanoid amides of serotonin on tyrosinase inhibition.

Takahashi T, Miyazawa M.

Bioorg Med Chem Lett. 2011 Apr 1;21(7):1983-6. doi: 10.1016/j.bmcl.2011.02.028. Epub 2011 Feb 13.

PMID:
21377874
3.

Tyrosinase inhibitory effects and antioxidative activities of novel cinnamoyl amides with amino acid ester moiety.

Fan Q, Jiang H, Yuan ED, Zhang JX, Ning ZX, Qi SJ, Wei QY.

Food Chem. 2012 Sep 15;134(2):1081-7. doi: 10.1016/j.foodchem.2012.03.021. Epub 2012 Mar 16.

PMID:
23107731
4.

Synthesis, antioxidant capacity, and structure-activity relationships of tri-O-methylnorbergenin analogues on tyrosinase inhibition.

Kashima Y, Miyazawa M.

Bioorg Med Chem Lett. 2013 Dec 15;23(24):6580-4. doi: 10.1016/j.bmcl.2013.10.066. Epub 2013 Nov 7.

PMID:
24268551
5.

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 1;22(13):3279-84. doi: 10.1016/j.bmc.2014.04.060. Epub 2014 May 15.

PMID:
24857777
6.

Synthesis and biological evaluation of bergenin analogues as mushroom tyrosinase inhibitors.

Kashima Y, Miyazawa M.

Arch Pharm Res. 2012 Sep;35(9):1533-41. doi: 10.1007/s12272-012-0903-3. Epub 2012 Oct 9.

PMID:
23054709
7.

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 1;21(7):2156-62. doi: 10.1016/j.bmc.2012.12.054. Epub 2013 Jan 11.

PMID:
23391365
8.

Tyrosinase inhibitory effect of benzoic acid derivatives and their structure-activity relationships.

Khan SB, Hassan Khan MT, Jang ES, Akhtar K, Seo J, Han H.

J Enzyme Inhib Med Chem. 2010 Dec;25(6):812-7. doi: 10.3109/14756366.2010.482529. Epub 2010 May 17.

PMID:
20476840
9.

Synthesis and evaluation of 2(3H)-thiazole thiones as tyrosinase inhibitors.

Emami S, Hosseinimehr SJ, Shahrbandi K, Enayati AA, Esmaeeli Z.

Arch Pharm (Weinheim). 2012 Aug;345(8):629-37. doi: 10.1002/ardp.201200028. Epub 2012 Apr 25.

PMID:
22532401
10.

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. doi: 10.1016/j.bmcl.2012.10.050. Epub 2012 Oct 17.

PMID:
23142612
11.

Rational design and synthesis of 4-o-substituted phenylmethylenethiosemicarbazones as novel tyrosinase inhibitors.

Yi W, Cao R, Chen Z, Yu L, Wen H, Yan Q, Ma L, Song H.

Chem Pharm Bull (Tokyo). 2010 May;58(5):752-4.

12.

Biological evaluation of coumarin derivatives as mushroom tyrosinase inhibitors.

Liu J, Wu F, Chen L, Zhao L, Zhao Z, Wang M, Lei S.

Food Chem. 2012 Dec 15;135(4):2872-8. doi: 10.1016/j.foodchem.2012.07.055. Epub 2012 Jul 24.

PMID:
22980884
13.

Anti-tyrosinase, antioxidant, and antibacterial activities of novel 5-hydroxy-4-acetyl-2,3-dihydronaphtho[1,2-b]furans.

Xia L, Idhayadhulla A, Lee YR, Wee YJ, Kim SH.

Eur J Med Chem. 2014 Oct 30;86:605-12. doi: 10.1016/j.ejmech.2014.09.025. Epub 2014 Sep 9.

PMID:
25218909
14.

Phenylethylamide and phenylmethylamide derivatives as new tyrosinase inhibitors.

Le Mellay-Hamon V, Criton M.

Biol Pharm Bull. 2009 Feb;32(2):301-3.

15.

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;49:245-52. doi: 10.1016/j.ejmech.2012.01.019. Epub 2012 Jan 24.

PMID:
22301213
16.

Design and synthesis of biphenyl derivatives as mushroom tyrosinase inhibitors.

Bao K, Dai Y, Zhu ZB, Tu FJ, Zhang WG, Yao XS.

Bioorg Med Chem. 2010 Sep 15;18(18):6708-14. doi: 10.1016/j.bmc.2010.07.062. Epub 2010 Aug 1.

PMID:
20729091
17.

Novel vitamin E derivative with 4-substituted resorcinol moiety has both antioxidant and tyrosinase inhibitory properties.

Shimizu K, Kondo R, Sakai K, Takeda N, Nagahata T, Oniki T.

Lipids. 2001 Dec;36(12):1321-6.

PMID:
11834083
18.
19.

Synthesis and evaluation of 2',4',6'-trihydroxychalcones as a new class of tyrosinase inhibitors.

Jun N, Hong G, Jun K.

Bioorg Med Chem. 2007 Mar 15;15(6):2396-402. Epub 2007 Jan 17.

PMID:
17267225
20.

Microwave-assisted synthesis and tyrosinase inhibitory activity of chalcone derivatives.

Liu J, Chen C, Wu F, Zhao L.

Chem Biol Drug Des. 2013 Jul;82(1):39-47. doi: 10.1111/cbdd.12126.

PMID:
23461881

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