Synthesis and Biological Evaluation of Chalcones having Heterosubstituent(s)

Chalcones and their synthetic analogues appear to have the same binding site of tubuline as phenstatin, combretastatin steganacin and podophylotoxin and are therefore capable to inhibit cancer cell proliferation. The phenyl rings with appropriate substitutions maintain a fixed distance between two c...

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Detalles Bibliográficos
Autores principales: Sweety, Kumar, S., Nepali, K., Sapra, S., Suri, O. P., Dhar, K. L., Sarma, G. S., Saxena, A. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Short Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178988/
https://www.ncbi.nlm.nih.gov/pubmed/21969759
http://dx.doi.org/10.4103/0250-474X.84602

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178988/
https://www.ncbi.nlm.nih.gov/pubmed/21969759
http://dx.doi.org/10.4103/0250-474X.84602

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