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A One-Pot Three-Component Synthesis and Investigation of the In Vitro Mechanistic Anticancer Activity of Highly Functionalized Spirooxindole-Pyrrolidine Heterocyclic Hybrids
Authors:Raju Suresh Kumar  Dhaifallah M. Al-thamili  Abdulrahman I. Almansour  Natarajan Arumugam  Faruq Mohammad
Affiliation:Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia; (D.M.A.-t.); (A.I.A.); (N.A.); (F.M.)
Abstract:With an aim to develop more effective and affordable anticancer agents possessing a unique mechanism of action, we designed and synthesized derivatives of spirooxindole-pyrrolidine heterocyclic hybrids in good yields through a one-pot three-component (3+2) cycloaddition strategy. The synthesized compounds were characterized thoroughly for the physicochemical properties by making use of FT-IR, NMR spectroscopy, and mass spectrometry. Further, these compounds have been evaluated for the influence of anticancer activity against HepG2 cells up to 200 µg/mL concentration. The highly active molecular scaffold was tested for the in-depth mechanistic studies, and it was found that the major pathway of cell death is apoptosis which occurs through the induction of reactive oxygen species followed by the involvement of caspases.
Keywords:multicomponent reaction   functionalized spirooxindole-pyrrolidine hybrids   anticancer activity   controlled cell death   apoptosis   ROS generation   caspase-3 activity
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