Molecular docking and inhibition of matrix metalloproteinase-2 by novel difluorinatedbenzylidene curcumin analog

We recently described the synthesis and characterization of a novel difluorinatedbenzylidene analog of curcumin, commonly referred as CDF, which demonstrated significantly enhanced bioavailability and in vivo anticancer activity. CDF targets many factors similar to curcumin, albeit with more potency...

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Publicat a:Am J Transl Res
Autors principals: Ahmad, Aamir, Sayed, Afreen, Ginnebaugh, Kevin R, Sharma, Vivek, Suri, Anita, Saraph, Arundhati, Padhye, Subhash, Sarkar, Fazlul H
Format: Artigo
Idioma:Inglês
Publicat: e-Century Publishing Corporation 2015
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4399093/
https://ncbi.nlm.nih.gov/pubmed/25901198
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