Synthesis, antitubercular and anticancer activity of new Baylis–Hillman adduct-derived N-cinnamyl-substituted isatin derivatives

Baylis–Hillman adduct-derived N-cinnamyl-substituted isatin derivatives were synthesized and evaluated for their antitubercular activity on Mycobacterium tuberculosis H(37)Rv strain ATCC 27294 by agar dilution method. Anticancer activity for the same compounds was also screened on four different cel...

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Detalles Bibliográficos
Autores principales: Kumar, Sriramoju Bharath, Ravinder, Mettu, Kishore, Golla, Jayathirtha Rao, Vaidya, Yogeeswari, Perumal, Sriram, Darmarajan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2013
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080103/
https://www.ncbi.nlm.nih.gov/pubmed/32214765
http://dx.doi.org/10.1007/s00044-013-0787-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080103/
https://www.ncbi.nlm.nih.gov/pubmed/32214765
http://dx.doi.org/10.1007/s00044-013-0787-x

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