Design, Synthesis, Bioactivity, and Docking Studies of Isatin-Hydrazone Derivatives as Potential CDK-2 Inhibitors

These novel isatin-hydrazone derivatives, particularly 2e, 2f, and 2h, could be used as potential anticancer agents that inhibit CDK2 kinase activity.

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Publication Details

Journal
Anti-Cancer Agents in Medicinal Chemistry
Published
2026-01-15
DOI
https://doi.org/10.2174/0118715206420750251029040513
Primary Topic
Cancer-related Molecular Pathways
Type
article
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article

Design, Synthesis, Bioactivity, and Docking Studies of Isatin-Hydrazone Derivatives as Potential CDK-2 Inhibitors

Kaige Guo, Xiaofen Liao, Ye Tao, Guobing Yan
Anti-Cancer Agents in Medicinal Chemistry
Cancer-related Molecular Pathways
article

Design, Synthesis, Bioactivity, and Docking Studies of Isatin-Hydrazone Derivatives as Potential CDK-2 Inhibitors

Kaige Guo, Xiaofen Liao, Ye Tao, Guobing Yan
article en

Abstract

These novel isatin-hydrazone derivatives, particularly 2e, 2f, and 2h, could be used as potential anticancer agents that inhibit CDK2 kinase activity.

Anti-Cancer Agents in Medicinal ChemistryVol. 26
Shaanxi Provincial People's Hospital (CN), Jiyang College of Zhejiang A&F University (CN)
Openalex Percentile: Top 78%
Cancer-related Molecular Pathways
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Design, Synthesis, Bioactivity, and Docking Studies of Isatin-Hydrazone Derivatives as Potential CDK-2 Inhibitors — Kaige Guo, Xiaofen Liao, et al. · Anti-Cancer Agents in Medicinal Chemistry (2026) | TGRS Research Map | TGRS