Design, Molecular Docking, Synthesis and Evaluation of New Isatin Derivatives Bearing Pyridine Moiety as Potential Tyrosine Kinase Inhibitors
Ibrahim, N., Mahdi, M., Raauf, A. (2022). Design, Molecular Docking, Synthesis and Evaluation of New Isatin Derivatives Bearing Pyridine Moiety as Potential Tyrosine Kinase Inhibitors. EKB Journal Management System, 65(2), 9-18. doi: 10.21608/ejchem.2021.72747.3607
Noor Waleed Ibrahim; Monther Mahdi; Ayad Mohammed Rasheed Raauf. "Design, Molecular Docking, Synthesis and Evaluation of New Isatin Derivatives Bearing Pyridine Moiety as Potential Tyrosine Kinase Inhibitors". EKB Journal Management System, 65, 2, 2022, 9-18. doi: 10.21608/ejchem.2021.72747.3607
Ibrahim, N., Mahdi, M., Raauf, A. (2022). 'Design, Molecular Docking, Synthesis and Evaluation of New Isatin Derivatives Bearing Pyridine Moiety as Potential Tyrosine Kinase Inhibitors', EKB Journal Management System, 65(2), pp. 9-18. doi: 10.21608/ejchem.2021.72747.3607
Ibrahim, N., Mahdi, M., Raauf, A. Design, Molecular Docking, Synthesis and Evaluation of New Isatin Derivatives Bearing Pyridine Moiety as Potential Tyrosine Kinase Inhibitors. EKB Journal Management System, 2022; 65(2): 9-18. doi: 10.21608/ejchem.2021.72747.3607

Design, Molecular Docking, Synthesis and Evaluation of New Isatin Derivatives Bearing Pyridine Moiety as Potential Tyrosine Kinase Inhibitors

Egyptian Journal of Chemistry
Article 2, Volume 65, Issue 2, February 2022, Page 9-18  XML PDF (978.47 K)
Document Type: Original Article
DOI: 10.21608/ejchem.2021.72747.3607
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Authors
Noor Waleed Ibrahim email orcid 1; Monther Mahdiorcid 2; Ayad Mohammed Rasheed Raauforcid 3
1Department of Pharmaceutical Chemistry, College of Pharmacy, Mustansiriyah University, Baghdad- Iraq.
2pharmaceutical chemistry department, college of pharmacy, Mustansiriyah University, Baghdad- Iraq.
3Department of Pharmaceutical Chemistry, College of Pharmacy, Mustansiriyah University, Baghdad-Iraq.
Abstract
A series of new 1-(3-imino-2-oxoindolin-5-yl)-3-phenylurea derivatives were synthesized starting from 5-aminoisatin; as a part of our program to compose multicomponent hybrid templates with potential pharmaceutical recognition and evaluate them as inhibitors of receptor tyrosine kinase. The proposed chemicals were synthesized and purified satisfactorily; They were classified and identified using a variety of methods: melting point, IR spectroscopy, 1H-NMR and13C-NMR; The effectiveness of these novel chemicals was tested for their in vitro cytotoxic activity and In silico tyrosine kinase selectivity through molecular docking via GOLD Suite (v.5.7.1); There is a good agreement between our docked results and the experimental results (In vitro study) since the compound 3a was the most potent cytotoxic scaffold shows the highest docking results and at the same time showing a promising antitumor activity among the tested compounds when tested against (A549) cancer cell lines by the MTT assay with IC50= 30.4 μM in comparison with erlotinib. Furthermore, using SWISS ADME, the drug likeness of these selected anti-proliferative drugs was anticipated based on their pharmacokinetics profiles. By not violating Lipinski's rule of five, the anti-proliferative drugs were determined to be orally safe. This study proposed a method for developing effective anti-proliferative drugs that target their target enzyme.
Keywords
5-Aminoisatin; Docking; ADME; GOLD; Lipinski rule
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