Synthesis and Characterization of Novel 1,2,3-Triazole linked Quinoline-based Thiazolidine-2,4-dione Derivatives as Potential Anticancer Agents and their Molecular Docking Studies

Novel hybrid molecules incorporating 1,2,3-triazole linked quinoline-based thiazolidine-2,4-dione derivatives (9a-l) were synthesized and validated through various 1H NMR, 13C NMR and ESI-MS. All the synthesized hybrid compounds were assessed for their anticancer activity against two cancer cell lines, MCF-7 and HEPG2, utilizing the MTT assay with doxorubicin as the standard reference drug. In comparison to the standard, compounds 9l, 9h, 9k, 9d and 9b exhibited superior activity against the tested cancer cell lines, MCF-7 and HEPG2. Additionally, molecular docking studies were conducted on the novel derivatives 9a-l against dihydrofolate reductase (DHFR), revealing a correlation between the molecular docking results and the observed anticancer activity.

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Publication Details

Journal
Asian Journal of Chemistry
Published
2025-02-28
DOI
https://doi.org/10.14233/ajchem.2025.33432
Primary Topic
Synthesis and biological activity
Type
article
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article

Synthesis and Characterization of Novel 1,2,3-Triazole linked Quinoline-based Thiazolidine-2,4-dione Derivatives as Potential Anticancer Agents and their Molecular Docking Studies

Dokku Sivaramakrishna, Ravada Kishore, Ananda Kumar Jami, Praveen Kumar Edigi et al.
Asian Journal of Chemistry
Synthesis and biological activity
article

Synthesis and Characterization of Novel 1,2,3-Triazole linked Quinoline-based Thiazolidine-2,4-dione Derivatives as Potential Anticancer Agents and their Molecular Docking Studies

Dokku Sivaramakrishna, Ravada Kishore, Ananda Kumar Jami, Praveen Kumar Edigi, Sreenivas Sunkara
article en

Abstract

Novel hybrid molecules incorporating 1,2,3-triazole linked quinoline-based thiazolidine-2,4-dione derivatives (9a-l) were synthesized and validated through various 1H NMR, 13C NMR and ESI-MS. All the synthesized hybrid compounds were assessed for their anticancer activity against two cancer cell lines, MCF-7 and HEPG2, utilizing the MTT assay with doxorubicin as the standard reference drug. In comparison to the standard, compounds 9l, 9h, 9k, 9d and 9b exhibited superior activity against the tested cancer cell lines, MCF-7 and HEPG2. Additionally, molecular docking studies were conducted on the novel derivatives 9a-l against dihydrofolate reductase (DHFR), revealing a correlation between the molecular docking results and the observed anticancer activity.

Asian Journal of ChemistryVol. 37(3)
Central Tobacco Research Institute (IN), GITAM University (IN), Osmania University (IN)
Openalex Percentile: Top 97%
Synthesis and biological activity
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