Solvent solute interaction (IEFPCM model), Michael addition-based anticancer drug synthesis, FTIR, NMR, and UV–visible investigations of spirooxindole-pyranoindole (2AIPC) − in vitro and in silico anti-cancer activity

Author:

Manikandan P,Kumar M.,Swarnamughi P.,Asif MohdORCID,Nasibullah Malik,Jeba Reeda V.S.,Khaled Jamal M,Muthu S.ORCID

Funder

King Saud University

Publisher

Elsevier BV

Reference90 articles.

1. Lewis base-catalyzed synthesis of highly functionalized spirooxindole-pyranopyrazoles and their in vitro anticancer studies;Asif;Med. Chem. Res.,2023

2. Novel functionalized spiro [Indoline-3,5′-pyrroline]-2,2′dione derivatives: synthesis, characterization, drug-likeness, ADME, and anticancer potential;Asif;Int. J. Mol. Sci.,2023

3. Synthesis of Functionalized 2′,5-Oxo-spiro[furan-2,3′-indoline]-3-carboxylate derivatives as antiproliferative agents: ADMET studies, and molecular docking against P2Y12 inhibitors;Asif;Chem. Select,2023

4. A perspective of the amide group containing fda approved anticancer drugs from 2021–2022 (a review);Asif;Russian J. Bioorg. Chem.,2023

5. Propagative isatin in organic synthesis of spirooxindoles through catalysis;Asif;Tetrahedron,2023

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