Research Article | Volume: 8, Issue: 7, July, 2018

Synthesis, Biological Evaluation, and Docking Analysis of Methyl Hydroquinone and Bromo Methyl Hydroquinone as Potent Cyclooxygenase (COX-1 and COX-2) Inhibitors

Nursamsiar Aiyi Asnawi Rahmana E. Kartasasmita Slamet Ibrahim Daryono Hadi Tjahjono   

Open Access   

Published:  Jul 30, 2018

DOI: 10.7324/JAPS.2018.8703
Abstract

NSAIDs reduce inflammation and relieve fever and pain by blocking enzymes and proteins but may cause side effects and complications by their use. It is therefore important for any molecular modification to enhance their pharmacological properties. In the present investigation, synthesis, biological evaluation, and molecular docking were performed for both methyl hydroquinone (1) and its brominated compound (2) to evaluate their anti-inflammatory activity against cyclooxygenase protein as a model compound and the data compared with its native ligands. Bromination of methyl hydroquinone using dichloromethane as solvent gave the highest yield. In vitro COX-1/COX-2 inhibition studies showed that compound 2 was a more potent COX inhibitor than compound 1. The brominated compound (2) showed lower binding energy and RMSD values compared to methyl hydroquinone. Analysis of protein and ligand binding revealed that both 1 and 2 fitted into the active site and interacted with protein amino acid residues Tyr385 and Met522 in COX-1 and Tyr385, Ser530, Val523, Ala527, and Leu384 in COX-2. Substitution of bromine plays an important role in the anti-inflammatory activity of methyl hydroquinone.


Keyword:     Bromination Cyclooxygenase Hydroquinone Inflammation NSAIDs.


Citation:

Nursamsiar, Asnawi A, Kartasasmita RE, Ibrahim S, Tjahjono DH. Synthesis, Biological Evaluation, and Docking Analysis of Methyl Hydroquinone and Bromo Methyl Hydroquinone as Potent Cyclooxygenase (COX-1 and COX-2) Inhibitors. J App Pharm Sci, 2018; 8(07): 016-020.

Copyright: © The Author(s). This is an open-access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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