Abdul Muhaimen Amjed Adnan, Monther Faisal Mahdi, Ayad Kareem Khan
Abdul Muhaimen Amjed Adnan1, Monther Faisal Mahdi2, Ayad Kareem Khan2
1Department of Pharmacy, Baghdad College of Medical Science, Baghdad, Iraq.
2Department of Pharmaceutical Chemistry, College of Pharmacy, Mustansiriyah University, Baghdad-Iraq.
Volume - 14,
Issue - 3,
Year - 2021
New 2-methyl benzimidazole derivatives were prepared and evaluated as possible inhibitor agents for cyclooxygenase-2 (COX-2). The synthesized derivatives structures have been recognized according to their spectral FT-IR, 1H-NMR data and physical properties. The newly synthesized compounds were inspected in vivo for their anti-inflammation efficiency using egg-white stimulated edema of paw method regarding the effect of propylene glycol 50%v/v as a control group. Ibuprofen (10mg/kg i.p.) was chosen as a reference ligand. New compounds exhibit a significant in vivo anti-inflammatory efficacy approached with ibuprofen as a reference drug. Selective evaluation of cyclooxygenase-2 by stimulating molecular cohesion through (GOLD suite v.5.6.2). All the investigated compounds via molecular docking showed significant more activities comparable with diclofenac and ibuprofen as referenced drugs. ADME studies were performed to estimate site of absorption, bioavailability, topological polar surface area and drug-likeness and it appeared that all synthesized compounds absorbed from GIT.
Cite this article:
Abdul Muhaimen Amjed Adnan, Monther Faisal Mahdi, Ayad Kareem Khan. New 2-Methyl Benzimidazole Derivatives bearing 4-Thiazolidinone Heterocyclic Rings: Synthesis, Preliminary Pharmacological Assessment and Docking Studies. Research J. Pharm. and Tech 2021; 14(3):1515-1520. doi: 10.5958/0974-360X.2021.00269.9
Abdul Muhaimen Amjed Adnan, Monther Faisal Mahdi, Ayad Kareem Khan. New 2-Methyl Benzimidazole Derivatives bearing 4-Thiazolidinone Heterocyclic Rings: Synthesis, Preliminary Pharmacological Assessment and Docking Studies. Research J. Pharm. and Tech 2021; 14(3):1515-1520. doi: 10.5958/0974-360X.2021.00269.9 Available on: https://rjptonline.org/AbstractView.aspx?PID=2021-14-3-58
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