Synthesis,characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel schiff bases derived from 1-(2-ketoiminoethyl)piperazines
Some novel Schiff bases derived from 1-(2-ketoiminoethyl)piperazines were synthesized and characterized by mass spectroscopy, FTIR, UV-Visible, (1)H and (13)C-NMR. The compounds were tested for inhibitory activities on human acetylcholinesterase (hAChE), antioxidant activities, acute oral toxicity a...
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my.um.eprints.51952019-01-30T00:50:27Z http://eprints.um.edu.my/5195/ Synthesis,characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel schiff bases derived from 1-(2-ketoiminoethyl)piperazines Salga, S.M. Hadi, A.H.A. Sukumaran, S.D. Buckle, M.J.C. Wai, L.K. Abdelwahab, S.I. Abdullah, M.A. Ali, Hapipah Mohd QD Chemistry Some novel Schiff bases derived from 1-(2-ketoiminoethyl)piperazines were synthesized and characterized by mass spectroscopy, FTIR, UV-Visible, (1)H and (13)C-NMR. The compounds were tested for inhibitory activities on human acetylcholinesterase (hAChE), antioxidant activities, acute oral toxicity and further studied by molecular modeling techniques. The study identified the compound (DHP) to have the highest activity among the series in hAChE inhibition and DPPH assay while the compound LP revealed the highest activity in the FRAP assay. The hAChE inhibitory activity of DHP is comparable with that of propidium, a known AChE inhibitor. This high activity of DHP was checked by molecular modeling which showed that DHP could not be considered as a bivalent ligand due to its incapability to occupy the esteratic site (ES) region of the 3D crystal structure of hAChE. The antioxidant study unveiled varying results in 1,1-diphenyl-1-picrylhydrazyl (DPPH) and ferric reducing antioxidant power (FRAP) assays. This indicates mechanistic variations of the compounds in the two assays. The potential therapeutic applications and safety of these compounds were suggested for use as human acetylcholinesterase inhibitors and antioxidants. 2011 Article PeerReviewed application/pdf en http://eprints.um.edu.my/5195/1/Salga-2011-Synthesis%2C_Character.pdf Salga, S.M. and Hadi, A.H.A. and Sukumaran, S.D. and Buckle, M.J.C. and Wai, L.K. and Abdelwahab, S.I. and Abdullah, M.A. and Ali, Hapipah Mohd (2011) Synthesis,characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel schiff bases derived from 1-(2-ketoiminoethyl)piperazines. Molecules, 16 (11). pp. 9316-9330. ISSN 1420-3049 http://www.mdpi.com/1420-3049/16/11/9316/pdf 10.3390/molecules16119316 |
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QD Chemistry Salga, S.M. Hadi, A.H.A. Sukumaran, S.D. Buckle, M.J.C. Wai, L.K. Abdelwahab, S.I. Abdullah, M.A. Ali, Hapipah Mohd Synthesis,characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel schiff bases derived from 1-(2-ketoiminoethyl)piperazines |
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Some novel Schiff bases derived from 1-(2-ketoiminoethyl)piperazines were synthesized and characterized by mass spectroscopy, FTIR, UV-Visible, (1)H and (13)C-NMR. The compounds were tested for inhibitory activities on human acetylcholinesterase (hAChE), antioxidant activities, acute oral toxicity and further studied by molecular modeling techniques. The study identified the compound (DHP) to have the highest activity among the series in hAChE inhibition and DPPH assay while the compound LP revealed the highest activity in the FRAP assay. The hAChE inhibitory activity of DHP is comparable with that of propidium, a known AChE inhibitor. This high activity of DHP was checked by molecular modeling which showed that DHP could not be considered as a bivalent ligand due to its incapability to occupy the esteratic site (ES) region of the 3D crystal structure of hAChE. The antioxidant study unveiled varying results in 1,1-diphenyl-1-picrylhydrazyl (DPPH) and ferric reducing antioxidant power (FRAP) assays. This indicates mechanistic variations of the compounds in the two assays. The potential therapeutic applications and safety of these compounds were suggested for use as human acetylcholinesterase inhibitors and antioxidants. |
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Article |
author |
Salga, S.M. Hadi, A.H.A. Sukumaran, S.D. Buckle, M.J.C. Wai, L.K. Abdelwahab, S.I. Abdullah, M.A. Ali, Hapipah Mohd |
author_facet |
Salga, S.M. Hadi, A.H.A. Sukumaran, S.D. Buckle, M.J.C. Wai, L.K. Abdelwahab, S.I. Abdullah, M.A. Ali, Hapipah Mohd |
author_sort |
Salga, S.M. |
title |
Synthesis,characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel schiff bases derived from 1-(2-ketoiminoethyl)piperazines |
title_short |
Synthesis,characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel schiff bases derived from 1-(2-ketoiminoethyl)piperazines |
title_full |
Synthesis,characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel schiff bases derived from 1-(2-ketoiminoethyl)piperazines |
title_fullStr |
Synthesis,characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel schiff bases derived from 1-(2-ketoiminoethyl)piperazines |
title_full_unstemmed |
Synthesis,characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel schiff bases derived from 1-(2-ketoiminoethyl)piperazines |
title_sort |
synthesis,characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel schiff bases derived from 1-(2-ketoiminoethyl)piperazines |
publishDate |
2011 |
url |
http://eprints.um.edu.my/5195/1/Salga-2011-Synthesis%2C_Character.pdf http://eprints.um.edu.my/5195/ http://www.mdpi.com/1420-3049/16/11/9316/pdf |
_version_ |
1643687510691282944 |
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13.18916 |