Anti-inflammatory trends of new benzimidazole derivatives
Aim: In present study, the anti-inflammatory activities of a new series of benzimidazole derivatives were studied, investigating their inhibition of secretory phospholipase A2, lipoxygenase, COXs and lipopolysaccharide-induced secretion of TNF-α and IL-6 in mouse RAW264.7 macrophages. Results: Synth...
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my.uniten.dspace-34672017-10-27T01:53:20Z Anti-inflammatory trends of new benzimidazole derivatives Bukhari, S.N.A. Lauro, G. Jantan, I. Chee, C.F. Amjad, M.W. Bifulco, G. Sher, H. Abdullah, I. Rahman, N.A. Aim: In present study, the anti-inflammatory activities of a new series of benzimidazole derivatives were studied, investigating their inhibition of secretory phospholipase A2, lipoxygenase, COXs and lipopolysaccharide-induced secretion of TNF-α and IL-6 in mouse RAW264.7 macrophages. Results: Synthesized compounds effectively inhibited proinflammatory enzymes and cytokines. Conclusion: A strong inhibition of secretory phospholipases A2 was exhibited by benzimidazole derivatives with trifluoromethyl and methoxy substitutions at position 4 of attached phenyl, whereas compound 8 containing pyridine ring substituted with amino group showed very potent 5-lipoxygenase inhibition. Molecular docking experiments were carried out to elucidate the molecular basis of the observed inhibitory activities. © 2016 Future Science Ltd. 2017-10-27T00:35:14Z 2017-10-27T00:35:14Z 2016 Article 10.4155/fmc-2016-0062 en Future Medicinal Chemistry Volume 8, Issue 16, October 2016, Pages 1953-1967 |
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Aim: In present study, the anti-inflammatory activities of a new series of benzimidazole derivatives were studied, investigating their inhibition of secretory phospholipase A2, lipoxygenase, COXs and lipopolysaccharide-induced secretion of TNF-α and IL-6 in mouse RAW264.7 macrophages. Results: Synthesized compounds effectively inhibited proinflammatory enzymes and cytokines. Conclusion: A strong inhibition of secretory phospholipases A2 was exhibited by benzimidazole derivatives with trifluoromethyl and methoxy substitutions at position 4 of attached phenyl, whereas compound 8 containing pyridine ring substituted with amino group showed very potent 5-lipoxygenase inhibition. Molecular docking experiments were carried out to elucidate the molecular basis of the observed inhibitory activities. © 2016 Future Science Ltd. |
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Article |
author |
Bukhari, S.N.A. Lauro, G. Jantan, I. Chee, C.F. Amjad, M.W. Bifulco, G. Sher, H. Abdullah, I. Rahman, N.A. |
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Bukhari, S.N.A. Lauro, G. Jantan, I. Chee, C.F. Amjad, M.W. Bifulco, G. Sher, H. Abdullah, I. Rahman, N.A. Anti-inflammatory trends of new benzimidazole derivatives |
author_facet |
Bukhari, S.N.A. Lauro, G. Jantan, I. Chee, C.F. Amjad, M.W. Bifulco, G. Sher, H. Abdullah, I. Rahman, N.A. |
author_sort |
Bukhari, S.N.A. |
title |
Anti-inflammatory trends of new benzimidazole derivatives |
title_short |
Anti-inflammatory trends of new benzimidazole derivatives |
title_full |
Anti-inflammatory trends of new benzimidazole derivatives |
title_fullStr |
Anti-inflammatory trends of new benzimidazole derivatives |
title_full_unstemmed |
Anti-inflammatory trends of new benzimidazole derivatives |
title_sort |
anti-inflammatory trends of new benzimidazole derivatives |
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2017 |
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1644493541601181696 |
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13.214268 |