Design, synthesis, cytotoxic activities, and molecular docking of chalcone hybrids bearing 8-hydroxyquinoline moiety with dual tubulin/EGFR kinase inhibition-Reference-Cited by-同舟云学术

Design, synthesis, cytotoxic activities, and molecular docking of chalcone hybrids bearing 8-hydroxyquinoline moiety with dual tubulin/EGFR kinase inhibition

Published:2023-05 Issue: Volume:134 Page:106444
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Amin Mohammed M.,Abuo-Rahma Gamal El-Din A.,Shaykoon Montaser Sh. A.,Marzouk Adel A.,Abourehab Mohammed A.S.,Saraya Roshdy E.,Badr Mohamed,Sayed Ahmed M.,Beshr Eman A.M.

Funder

Umm Al-Qura University

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference107 articles.

1. Mechanisms of multidrug resistance in cancer chemotherapy;Bukowski;Int. J. Mol. Sci.,2020

2. Structure-activity relationships of 8-hydroxyquinoline-derived Mannich bases with tertiary amines targeting multidrug-resistant cancer;Pape;J. Med. Chem.,2022

3. Nitric oxide-donating and reactive oxygen species-responsive prochelators based on 8-hydroxyquinoline as anticancer agents;Zhang;Eur. J. Med. Chem.,2021

4. Ligand substituent effect on the cytotoxicity activity of two new copper (ii) complexes bearing 8-hydroxyquinoline derivatives: validated by MTT assay and apoptosis in MCF-7 cancer cell line (human breast cancer);Ali;RSC Adv.,2021

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