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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Main Authors: Bukhari, S.N.A., Lauro, G., Jantan, I., Chee, C.F., Amjad, M.W., Bifulco, G., Sher, H., Abdullah, I., Rahman, N.A.
Format: Article
Language:English
Published: 2017
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spelling 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
institution Universiti Tenaga Nasional
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country Malaysia
content_provider Universiti Tenaga Nasional
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description 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.
format 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.
spellingShingle 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
publishDate 2017
_version_ 1644493541601181696
score 13.214268