Synthesis and Biological Evaluation of Unsymmetrical Curcumin Analogues as Tyrosinase Inhibitors

Synthesis and biological evaluation of unsymmetrical curcumin analogues (UCAs) have been achieved. Tyrosinase inhibitory activities were found for most of the prepared synthetic UCAs. Among them, compounds containing 4-hydroxyl-substituted phenolic rings with C-2/C-4- or C-3/C-4-dihydroxyl-substitut...

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Vydáno v:Molecules
Hlavní autoři: Jiang, Yongfu, Du, Zhiyun, Xue, Guihua, Chen, Qian, Lu, Yujing, Zheng, Xi, Conney, Allan H., Zhang, Kun
Médium: Artigo
Jazyk:Inglês
Vydáno: MDPI 2013
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6269853/
https://ncbi.nlm.nih.gov/pubmed/23552906
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules18043948
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