Unravelling the Selectivity of 6,7‐Dimethyl Quinoxaline Analogs for Kinase Inhibition: An Insight towards the Development of Alzheimer's Therapeutics

• Published in: Chemistry & biodiversity Vol. 18; no. 11; pp. e2100364 - n/a
• Main Authors: Kumar Jain, Arvind, Gupta, Arindam, Karthikeyan, C., Trivedi, Piyush, Dutt Konar, Anita
• Format: Journal Article
• Language: English
• Published: Switzerland Wiley Subscription Services, Inc 01.11.2021
• Subjects: Alzheimer Disease - drug therapy; Alzheimer Disease - metabolism; Alzheimer's disease; Analogs; Aromatic compounds; Biological effects; docking studies; Drug Development; Dyrk Kinases; Electron density; Glycogen Synthase Kinase 3 beta - antagonists & inhibitors; Glycogen Synthase Kinase 3 beta - metabolism; halide derivatives of 6,7-dimethyl quinoxaline analogs; Humans; Imines; Inhibitors; Kinases; Ligands; Models, Molecular; Molecular modelling; Molecular Structure; Neurodegenerative diseases; Neuroprotective Agents - chemical synthesis; Neuroprotective Agents - chemistry; Neuroprotective Agents - pharmacology; Oxazole; Phosphorylation; Protein Kinase Inhibitors - chemical synthesis; Protein Kinase Inhibitors - chemistry; Protein Kinase Inhibitors - pharmacology; Protein Serine-Threonine Kinases - antagonists & inhibitors; Protein Serine-Threonine Kinases - metabolism; Protein-Tyrosine Kinases - antagonists & inhibitors; Protein-Tyrosine Kinases - metabolism; Quinoxaline; Quinoxalines; Quinoxalines - chemical synthesis; Quinoxalines - chemistry; Quinoxalines - pharmacology; Receptors; Selectivity; selectivity towards GSK3β receptors; Tau protein; selectivity towards GSK3β receptors; docking studies; halide derivatives of 6,7-dimethyl quinoxaline analogs
• ISSN: 1612-1872; 1612-1880
• DOI: 10.1002/cbdv.202100364

Untangling the most selective kinase inhibitors via pharmacological intervention remains one of the challenging affairs to date. In accordance to this drift, herein we describe the design and synthesis of a set of new heterocyclic analogs consisting of 6,7‐dimethyl Quinoxaline, appended to a connector, employing Schiff base strategy (Compounds I–IX). The compounds were characterized by various spectroscopic techniques and the kinase inhibition assay were performed on few prime members of the CMGC family namely the GSK3β, DYRK1A and CLK1 receptors, respectively, that have been known to be directly involved in hyperphosphorylation of Tau. Interestingly the biological evaluation results revealed that Compounds IV and V, with bromo/chloro functionalities in the aromatic core were advantaged of being highly selective towards the target GSK3β over others. To strengthen our analysis, we adopted molecular modelling studies, where compounds IV/V were redocked in the same grid 4AFJ, as that of the reference ligand, 5‐aryl‐4‐carboxamide‐1,3‐oxazole. Surprisingly, our investigation underpinned that for both the compounds IV/V, a primary H‐bonding existed between the designed molecules (IV/V) and Val 135 residue in the receptor GSK3β, in line with the reference ligand. We attribute this interaction to instigate potency in the compounds. Indeed the other non‐covalent interaction, between the derivative's aromatic nucleus and Arg 141/Thr 138 in the receptor GSK3β, might have been responsible for enhancing the selectivity in the targets. Overall, we feel that the present work depicts a logical demonstration towards fine tuning the efficacy of the inhibitors through systematic adjustment of electron density at appropriate positions in the aromatic ring be it the main quinoxaline or the other aromatic nucleus. Thus this pathway offers a convenient strategy for the development of efficient therapeutics for diversified neurodegenerative diseases like that of Alzheimer's.