Abstract
AbstractA facile single pot strategy was developed to synthesize a library of 17 arylpropenone aminochalcone conjugates involving two consecutive reactions, namely Michael addition and Claisen‐Schmidt condensation. These conjugates were screened for their in vitro anti‐proliferative potential against selected human cancer cell lines such as breast (MCF‐7 and MDA‐MB‐231), pancreatic (PANC‐1) and colorectal (CaCO2) adenocarcinoma cells. Among them, the conjugates 6 l and 6p exhibited good to moderate cytotoxicity with IC50 values ranging from 6.7 μM and 9.8 μM, respectively, against MCF‐7. Furthermore, these conjugates were found to exhibit G0/G1 cell cycle arrest. Moreover, Annexin‐FITC assay revealed that they induced apoptosis in a dose‐dependent manner which probably is responsible for their Cytotoxicity
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call