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Synthesis and Cytotoxic Evaluation of Monocarbonyl Analogs of Curcumin as Potential Anti‐Tumor Agents

[Table: see text] A series of mono‐carbonyl curcumin analogs with different substituents at the 4/4’‐position of the phenyl group were synthesized and screened for in vitro cytotoxicity against a panel of human cancer cell lines using a methyl thiazolyl tetrazolium assay. Several of the curcumin ana...

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Detalles Bibliográficos
Autores principales:	Pan, Zheer, Chen, Chengwei, Zhou, Yeli, Xu, Feng, Xu, Yaozeng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2016
Materias:	Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832843/ https://www.ncbi.nlm.nih.gov/pubmed/26846154 http://dx.doi.org/10.1002/ddr.21291

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