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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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Bibliografske podrobnosti
izdano v:Molecules
Main Authors: Jiang, Yongfu, Du, Zhiyun, Xue, Guihua, Chen, Qian, Lu, Yujing, Zheng, Xi, Conney, Allan H., Zhang, Kun
Format: Artigo
Jezik:Inglês
Izdano: MDPI 2013
Teme:
Online dostop: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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