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J Recept Signal Transduct Res ; 41(2): 153-158, 2021 Apr.
Article in English | MEDLINE | ID: mdl-32752909

ABSTRACT

MAP kinase is one of the important targets in the treatment of osteoarthritis, inflammation and cancer. Many p38 inhibitors with diverse chemical structures and modes of protein interaction have been designed on the basis of their ability to compete with ATP site or allosteric site for binding to MAP Kinase. This study involves the molecular docking of benzimidazoles containing 4H-chrome-4-one derivatives as potent inhibitors of the MAP kinase enzyme. The compounds were computationally designed and optimized with the molecular docking to investigate the interactions between the target compounds and the amino acid residues of the MAP Kinase. The inhibitory activities against human MAP kinase enzyme were investigated by molecular docking using the Autodock and discovery studio software. All the designed compounds were shown good binding energy when compared with the binging energies of standard drug Imatinib (anti-cancer). Among all the designed compounds, compound D1 and D6 have higher binding energy values when compared to standard drug. Here we also studied the molecular properties of designed compound using Molinspiration software. Further, we planned to synthesis these benzimidazole derivatives and screen for in-vitro and in-vivo of anti-cancer activity.


Subject(s)
Benzimidazoles/chemistry , Drug Design , Protein Kinase Inhibitors/chemistry , p38 Mitogen-Activated Protein Kinases/chemistry , Adenosine Triphosphate/chemistry , Allosteric Site/drug effects , Benzimidazoles/therapeutic use , Computer Simulation , Drug Screening Assays, Antitumor , Humans , Imatinib Mesylate , Molecular Docking Simulation , Molecular Structure , Neoplasms/drug therapy , Protein Kinase Inhibitors/therapeutic use , Structure-Activity Relationship , p38 Mitogen-Activated Protein Kinases/antagonists & inhibitors , p38 Mitogen-Activated Protein Kinases/therapeutic use , p38 Mitogen-Activated Protein Kinases/ultrastructure
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