Synthesis of novel triazoloquinoxaline‐pyrazole hybrids as antiproliferatives,EGFRinhibitors, and apoptosis inducers
Author:
Affiliation:
1. Pharmaceutical Organic Chemistry, Faculty of Pharmacy (Girls) Al‐Azhar University Cairo Egypt
2. Pharmaceutical Organic Chemistry, Faculty of Pharmacy (Boys) Al‐Azhar University Cairo Egypt
Publisher
Wiley
Subject
Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.4144
Reference31 articles.
1. Design and Synthesis of New Quinoxaline Derivatives as Anticancer Agents and Apoptotic Inducers
2. Design, Synthesis and Cytotoxic Evaluation of Novel Chalcone Derivatives Bearing Triazolo[4,3-a]-quinoxaline Moieties as Potent Anticancer Agents with Dual EGFR Kinase and Tubulin Polymerization Inhibitory Effects
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1. Design, synthesis and biological evaluation of newly triazolo-quinoxaline based potential immunomodulatory anticancer molecules;Journal of Molecular Structure;2024-02
2. Inherent efficacies of pyrazole-based derivatives for cancer therapy: the interface between experiment and in silico;Future Medicinal Chemistry;2023-09
3. Nitrogen‐Containing Heterocyclic Scaffolds as EGFR Inhibitors: Design Approaches, Molecular Docking, and Structure‐Activity Relationships;ChemistrySelect;2023-07-10
4. Synthesis, characterization and biological activity of Mn(II), Co(II), Ni(II), Cu(II) and Zn(II) complexes derived from Schiff base ligand quinoxaline-2-carboxaldehyde and 4-aminoantipyrine;Journal of Molecular Structure;2022-08
5. Recent Updates on the Anticancer Activity of Quinoxaline Hybrids (Jan. 2017-Jan. 2022);Current Topics in Medicinal Chemistry;2022-07
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