Novel Quinoline-3,4-dihydropyrimidinone Hybrids Privileged Scaffolds: Design, Synthesis, and Cytotoxic Evaluation
Mansour, B., El-Sayed, M., Massoud, M., Bayoumi, W. (2024). Novel Quinoline-3,4-dihydropyrimidinone Hybrids Privileged Scaffolds: Design, Synthesis, and Cytotoxic Evaluation. EKB Journal Management System, 7(1), -. doi: 10.21608/dusj.2024.248019.1031
Basem A Mansour; Magda A. El-Sayed; Mohammed Massoud; Waleed Bayoumi. "Novel Quinoline-3,4-dihydropyrimidinone Hybrids Privileged Scaffolds: Design, Synthesis, and Cytotoxic Evaluation". EKB Journal Management System, 7, 1, 2024, -. doi: 10.21608/dusj.2024.248019.1031
Mansour, B., El-Sayed, M., Massoud, M., Bayoumi, W. (2024). 'Novel Quinoline-3,4-dihydropyrimidinone Hybrids Privileged Scaffolds: Design, Synthesis, and Cytotoxic Evaluation', EKB Journal Management System, 7(1), pp. -. doi: 10.21608/dusj.2024.248019.1031
Mansour, B., El-Sayed, M., Massoud, M., Bayoumi, W. Novel Quinoline-3,4-dihydropyrimidinone Hybrids Privileged Scaffolds: Design, Synthesis, and Cytotoxic Evaluation. EKB Journal Management System, 2024; 7(1): -. doi: 10.21608/dusj.2024.248019.1031

Novel Quinoline-3,4-dihydropyrimidinone Hybrids Privileged Scaffolds: Design, Synthesis, and Cytotoxic Evaluation

Delta University Scientific Journal
Article 1, Volume 7, Issue 1, April 2024  XML PDF (413.5 K)
Document Type: Original research papers
DOI: 10.21608/dusj.2024.248019.1031
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Authors
Basem A Mansour email orcid 1; Magda A. El-Sayed2; Mohammed Massoud3; Waleed Bayoumi3
1Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Delta University for Science and Technology, International Coastal Road, Gamasa City, 35712, Egypt
2Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Horus University, New Damietta, 34518, Egypt
3Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Mansoura University, Mansoura 35516, Egypt
Abstract
Biologically active quinoline-3,4-dihydropyrimidin-2(1H)-one hybrids as novel monastrol analogs, were designed via molecular hybridization and structural modification rational. The synthesis was easily accessible via classical Biginelli reaction in good yields. Investigation of in vitro cytotoxicity was achieved through MTT cell line assay. The results revealed that the target derivatives showed a spectrum of potential cytotoxic effects on HepG-2, HCT-116, MCF-7, and PC3 cell lines, taking 5-FU as standard antitumor agents. Compounds 7e (R = tert-butoxy) and 7f (R = 2-methylpropyloxy) showed the greatest cytotoxic efficacy among the tested hybrids on the investigated cell lines; in which 7e showed IC50 values range of (11.57 μM - 19.05 μM), while 7f showed IC50 values range (14.16 μM - 19.96 μM), in comparison with the standard 5-FU (IC50 from 5.3 μM to 8.3 μM). The introduced quinoline-3,4-dihydropyrimidin-2(1H)-one hybrids with their readily straightforward structural modification, may serve as a potential cytotoxic antitumor candidate after suitable optimization.
Keywords
Monastrol; Quinoline; 3; 4-Dihydropyrimidin-2(1H)-one; Cytotoxicity
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