A series of spirooxindolopyrrolidine fused -styrylpiperidone heterocyclic hybrids has been synthesized in excellent yield via a domino multicomponent protocol that involves one-pot three component 1,3-dipolar cycloaddition and concomitant enamine reactions performed in an inexpensive ionic liquid, namely 1-butyl-3-methylimidazolium bromide ([bmim]Br). Compounds thus synthesized were evaluated for their cytotoxicity against U-937 tumor cells. Interestingly; compounds and exhibited a better cytotoxicity than the anticancer drug bleomycin. In addition; the effect of the synthesized compounds on the nuclear morphology of U937 FaDu cells revealed that treatment with compounds ⁻ led to their apoptotic cell death.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100567 | PMC |
http://dx.doi.org/10.3390/molecules23051094 | DOI Listing |
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