A novel Imatinib analog inhibitor of chronic myeloid leukemia: design, synthesis, and characterization. : Explanation of its folded conformation
Moreno-Fuquen, Rodolfo and Avellaneda-Tamayo, Juan F. and Arango-Daraviña, Kevin and Ellena, Javier and Kennedy, Alan R. (2024) A novel Imatinib analog inhibitor of chronic myeloid leukemia: design, synthesis, and characterization. : Explanation of its folded conformation. Royal Society Open Science. ISSN 2054-5703 (In Press) (https://doi.org/10.1098/rsos.241654)
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Abstract
Chronic Myeloid Leukemia (CML) is primarily treated using Imatinib mesylate, a tyrosine kinase inhibitor (TKI) targeting the BCR::ABL1 oncoprotein. However, the development of drug resistance and adverse side effects necessitates the exploration of alternative therapeutic agents. This study presents the synthesis and characterization of a novel Imatinib analog, 3-chloro-N-(2-methyl-5-((4-(pyridin-2-yl)pyrimidin-2-yl)amino)phenyl)benzamide (PAPP1). The compound’s structure was elucidated using X-ray crystallography and spectroscopic techniques, including NMR, IR, and UV/Vis. Crystallographic analysis reveals that PAPP1 consists of a phenyl-amino-pyridine-pyrimidine (PAPP) scaffold with substituted aromatic rings forming a nearly coplanar geometry. . Additionally, supramolecular interactions in the crystal are mediated by hydrogen bonds and dispersion forces, forming dimers and layered structures. Molecular docking studies demonstrate strong binding affinity to the ABL1 enzyme, with PAPP1 showing comparable binding energy to Imatinib, indicating its potential as a lead compound for further development. Computational studies, including molecular electrostatic potential and vibrational analysis, provide further support for the structural stability and bioactivity of PAPP1. These findings suggest that PAPP could be a promising scaffold for future CML drug design, offering a potential alternative to existing TKIs, and PAPP1 is a promising lead susceptible to optimization.
ORCID iDs
Moreno-Fuquen, Rodolfo, Avellaneda-Tamayo, Juan F., Arango-Daraviña, Kevin, Ellena, Javier and Kennedy, Alan R. ORCID: https://orcid.org/0000-0003-3652-6015;-
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Item type: Article ID code: 91764 Dates: DateEvent20 December 2024Published20 December 2024AcceptedSubjects: Medicine > Pharmacy and materia medica > Pharmaceutical chemistry Department: Faculty of Science > Pure and Applied Chemistry Depositing user: Pure Administrator Date deposited: 10 Jan 2025 11:20 Last modified: 10 Jan 2025 11:20 URI: https://strathprints.strath.ac.uk/id/eprint/91764