Novel Pyrido-Thiazolo-Pyrimidinone Hybrids targeting EGFRWT and EGFRT790M: Design, Synthesis, Anticancer Activity and docking simulation
Alasfoury, R., Nossier, E., El-Manawaty, M., Elzahabi, H. (2023). Novel Pyrido-Thiazolo-Pyrimidinone Hybrids targeting EGFRWT and EGFRT790M: Design, Synthesis, Anticancer Activity and docking simulation. EKB Journal Management System, 3(1), 112-119. doi: 10.21608/aijpms.2022.147229.1149
Rania A Alasfoury; Eman S Nossier; May El-Manawaty; Heba SA Elzahabi. "Novel Pyrido-Thiazolo-Pyrimidinone Hybrids targeting EGFRWT and EGFRT790M: Design, Synthesis, Anticancer Activity and docking simulation". EKB Journal Management System, 3, 1, 2023, 112-119. doi: 10.21608/aijpms.2022.147229.1149
Alasfoury, R., Nossier, E., El-Manawaty, M., Elzahabi, H. (2023). 'Novel Pyrido-Thiazolo-Pyrimidinone Hybrids targeting EGFRWT and EGFRT790M: Design, Synthesis, Anticancer Activity and docking simulation', EKB Journal Management System, 3(1), pp. 112-119. doi: 10.21608/aijpms.2022.147229.1149
Alasfoury, R., Nossier, E., El-Manawaty, M., Elzahabi, H. Novel Pyrido-Thiazolo-Pyrimidinone Hybrids targeting EGFRWT and EGFRT790M: Design, Synthesis, Anticancer Activity and docking simulation. EKB Journal Management System, 2023; 3(1): 112-119. doi: 10.21608/aijpms.2022.147229.1149

Novel Pyrido-Thiazolo-Pyrimidinone Hybrids targeting EGFRWT and EGFRT790M: Design, Synthesis, Anticancer Activity and docking simulation

Azhar International Journal of Pharmaceutical and Medical Sciences
Article 11, Volume 3, Issue 1, January 2023, Page 112-119  XML PDF (1 MB)
Document Type: Original research articles
DOI: 10.21608/aijpms.2022.147229.1149
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Authors
Rania A Alasfoury email 1; Eman S Nossierorcid 1; May El-Manawaty2; Heba SA Elzahabi1
1Pharmaceutical Medicinal Chemistry & Drug Design Department, Faculty of Pharmacy (Girls), Al-Azhar University, Cairo, Egypt
2Pharmacognosy department National Research Centre, Dokki, Cairo 12622, Egypt.
Abstract
Pyrido[2,3-d]pyrimidinones and thiazolo based scaffold were reported to exhibit valuable anticancer activity and inhibit EGFR tyrosine kinase receptors wild and mutant types as well. So new series of 6,8- diaryl pyrido[2,3-d]thiazolo[3,2-a]pyrimidinones 2a-c was synthesized and their chemical structures were confirmed through different spectral analyses including IR, 1HNMR, 13CNMR and mass spectroscopy. Anticancer evaluation was performed through screening for these compounds against A-549, PC-3, HCT-116, and MCF-7 cancerous cell lines at a dose of 100 in comparison with erlotinib. The antiproliferative activity revealed that compound 2a was excellent and approximately equipotent with the reference (IC50= 13.25 and 11.05 μM) which implicated that substitution at position 6 and 8 greatly affect the cytotoxic activity. Furthermore, the promising compound 2a was subjected to molecular docking analysis against EGFRWT and EGFRT790M kinases to examine the binding mode and elucidate the mechanism of the promising cytotoxic activity. Finally compound 2a has been shown to be good candidate that deserve further investigation.
Keywords
pyrido[2; 3-d]thiazolo[3; 2-a]pyrimidinones; anticancer; docking simulation
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