Docking, Molecular Dynamics Simulation and Synthesis of New Fenobam Analogues as mGlu5 Receptor Antagonists

Author(s): Abdollah Javidan, Mohammad Javad Taghizadeh, Seyed Ayoub Hosseini, Maryam Iman, Rahim Jafari

Journal Name: Combinatorial Chemistry & High Throughput Screening
Accelerated Technologies for Biotechnology, Bioassays, Medicinal Chemistry and Natural Products Research

Volume 19 , Issue 9 , 2016

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Background: Fenobam is a non-competitive mGluR5 antagonist as an anxiolytic agent.

Objective: In this research a new series of fenobam analogues containing thiazole moiety instead of imidazole ring were designed and synthesized.

Methods: The ureido-substituted products were synthesized from reaction of amino thiazole derivatives and isocyanate derivatives in dichloromethane solvent under microwave and ultrasonic irradiation condition. The synthesized compounds structures were established by means of IR, 1HNMR, 13CNMR spectroscopic data. Then, docking calculations were performed on the active site of mGLuR5 and compared to Fenobam as a reference drug by using AutoDock program. The molecular dynamics (MD) simulations were done using GROMACS 5.0.5.

Results: Docking studies suggested that all of the compounds possess better binding energy when compared to fenobam. The results of MD simulations might offer the binding mode of ligand (3b), accuracy of docking and the reliability of active conformations which obtained by AutoDock.

Conclusion: New derivatives of fenobam were designed and synthesized that have the better insilico results compared to fenobam and will evaluate in future studies.

Keywords: Isocyanates, fenobam, thiazole derivatives, synthesis, docking, molecular dynamics simulation.

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Article Details

Year: 2016
Page: [764 - 770]
Pages: 7
DOI: 10.2174/1386207319666160831150500
Price: $65

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