Biological evaluation of indolizine-chalcone hybrids as new anticancer agents

Chalcone Indolizine Aldol condensation
DOI: 10.1016/j.ejmech.2017.12.056 Publication Date: 2017-12-19T08:17:03Z
ABSTRACT
A new chemical space was explored based on an indolizine-chalcone hybrid, which was readily accessible by base-mediated aldol condensation of indolizine bearing a 7-acetyl group with various (hetero)aromatic aldehydes. Their anticancer effect was evaluated, revealing that indolizine-chalcone hybrids with 3,5-dimethoxyphenyl group (4h) or the halogen at the meta position (4j and 4l) could have the potential to induce the caspase-dependent apoptosis of human lymphoma cells.
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