Abstract
AbstractA one‐pot Kabachnik‐Fields reaction is used in the presence of magnesium triflate [Mg(OTf)2] as a catalyst between quinoline, diethyl phosphite (DEP), and substituted aldehydes to synthesize quinoline thioacetohydrazide α‐aminophosphonates (5 a‐f). Analytical and spectroscopic techniques identify the novel compounds. The cytotoxicity properties of the synthesized compounds were examined against HepG2 and MCF7 human cancer cells using the MTT assay. Some of the synthesized compounds exhibit potent anticancer activities. Compounds 5 e and 5 b exhibited the most promising activity against MCF7 human cancer cells, while compounds 5 c and 5 e were potent against HepG2 human cancer cells. Molecular docking experiments on the active compounds showed ring‐stacking interactions between compounds 5 b, 5 c, and 5 e with other proteins, which are compatible with other results.
Sign-in/Register to access full text options 
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 callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
