Unknown

Dataset Information

0

A One-Pot Three-Component Synthesis and Investigation of the In Vitro Mechanistic Anticancer Activity of Highly Functionalized Spirooxindole-Pyrrolidine Heterocyclic Hybrids.


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.

SUBMITTER: Kumar RS 

PROVIDER: S-EPMC7730040 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

A One-Pot Three-Component Synthesis and Investigation of the In Vitro Mechanistic Anticancer Activity of Highly Functionalized Spirooxindole-Pyrrolidine Heterocyclic Hybrids.

Kumar Raju Suresh RS   M Al-Thamili Dhaifallah D   Almansour Abdulrahman I AI   Arumugam Natarajan N   Mohammad Faruq F  

Molecules (Basel, Switzerland) 20201127 23


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  ...[more]

Similar Datasets

| S-EPMC7587566 | biostudies-literature
| S-EPMC7283928 | biostudies-literature
| S-EPMC6119554 | biostudies-literature
| S-EPMC7783807 | biostudies-literature
| S-EPMC6225336 | biostudies-literature
| S-EPMC9383709 | biostudies-literature
| S-EPMC6682060 | biostudies-literature
| S-EPMC7221748 | biostudies-literature
| S-EPMC9079859 | biostudies-literature
| S-EPMC6759581 | biostudies-literature