Biological evaluation of indolizine-chalcone hybrids as new anticancer agents

Biological evaluation of indolizine-chalcone hybrids as new anticancer agents Scaffold hybridization in generation of indenoindolones as anticancer agents that induce apoptosis with cell cycle arrest at G2/M phase 1,2,3-Triazole-Chalcone hybrids: Synthesis, in vitro cytotoxic activity and mechanistic investigation of apoptosis induction in multiple myeloma RPMI-8226 Spirooxindole-pyrrolidine heterocyclic hybrids promotes apoptosis through activation of caspase-3 Synthesis of imidazo[2,1-b][1,3,4]thiadiazole–chalcones as apoptosis inducing anticancer agents Synthesis of novel indole-thiazolidinone hybrid structures as promising scaffold with anticancer potential Synthesis and evaluation of indole-containing 3,5-diarylisoxazoles as potential pro-apoptotic antitumour agents Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione Synthesis and anticancer activity studies of indolylisoxazoline analogues Design and synthesis of new coumarin hybrids and insight into their mode of antiproliferative action