Synthesis and biological evaluation of flavonoids as antiacetyl-cholinesterase agent

A series of chalcones, a flavone and one flavanone were synthesized and elucidated structurally by IR and 1H NMR spectroscopies. The synthetic compounds were then screened for acetylcholinesterase inhibitory activity using thin layer chromatography (TLC) and microplate assays. In the TLC assay, only...

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Main Authors: Ibrahim, Saleh Nazifi, Amad, Farediah
Format: Article
Published: Penerbit UTM Press 2014
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author Ibrahim, Saleh Nazifi
Amad, Farediah
author_facet Ibrahim, Saleh Nazifi
Amad, Farediah
author_sort Ibrahim, Saleh Nazifi
collection ePrints
description A series of chalcones, a flavone and one flavanone were synthesized and elucidated structurally by IR and 1H NMR spectroscopies. The synthetic compounds were then screened for acetylcholinesterase inhibitory activity using thin layer chromatography (TLC) and microplate assays. In the TLC assay, only 2′-hydroxy-4-methoxychalcone and 2′-hydroxy-4′-O-prenyl-2,6-dichlorochalcone were found to show moderate and weak activity respectively against acetylcholinesterase (AchE) at 0.1 mM concentration compared to the control galanthamine. 4′-Hydroxy-2,6-dichlorochalcone, 2′-hydroxy-4-nitrochalcone, 2′-hydroxy-4-(dimethyl)aminochalcone and 2′-hydroxy-4-methoxychalcone showed moderate AchE inhibitory activity with percentage inhibition of 54.24, 46.14 and 49.32 % respectively in the microplate assay.
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spelling utm.eprints-627652017-11-01T04:17:08Z http://eprints.utm.my/62765/ Synthesis and biological evaluation of flavonoids as antiacetyl-cholinesterase agent Ibrahim, Saleh Nazifi Amad, Farediah Q Science A series of chalcones, a flavone and one flavanone were synthesized and elucidated structurally by IR and 1H NMR spectroscopies. The synthetic compounds were then screened for acetylcholinesterase inhibitory activity using thin layer chromatography (TLC) and microplate assays. In the TLC assay, only 2′-hydroxy-4-methoxychalcone and 2′-hydroxy-4′-O-prenyl-2,6-dichlorochalcone were found to show moderate and weak activity respectively against acetylcholinesterase (AchE) at 0.1 mM concentration compared to the control galanthamine. 4′-Hydroxy-2,6-dichlorochalcone, 2′-hydroxy-4-nitrochalcone, 2′-hydroxy-4-(dimethyl)aminochalcone and 2′-hydroxy-4-methoxychalcone showed moderate AchE inhibitory activity with percentage inhibition of 54.24, 46.14 and 49.32 % respectively in the microplate assay. Penerbit UTM Press 2014 Article PeerReviewed Ibrahim, Saleh Nazifi and Amad, Farediah (2014) Synthesis and biological evaluation of flavonoids as antiacetyl-cholinesterase agent. Jurnal Teknologi (Sciences and Engineering), 69 (1). pp. 97-102. ISSN 2180-3722 http://dx.doi.org/10.11113/jt.v69.2588 DOI:10.11113/jt.v69.2588
spellingShingle Q Science
Ibrahim, Saleh Nazifi
Amad, Farediah
Synthesis and biological evaluation of flavonoids as antiacetyl-cholinesterase agent
title Synthesis and biological evaluation of flavonoids as antiacetyl-cholinesterase agent
title_full Synthesis and biological evaluation of flavonoids as antiacetyl-cholinesterase agent
title_fullStr Synthesis and biological evaluation of flavonoids as antiacetyl-cholinesterase agent
title_full_unstemmed Synthesis and biological evaluation of flavonoids as antiacetyl-cholinesterase agent
title_short Synthesis and biological evaluation of flavonoids as antiacetyl-cholinesterase agent
title_sort synthesis and biological evaluation of flavonoids as antiacetyl cholinesterase agent
topic Q Science
work_keys_str_mv AT ibrahimsalehnazifi synthesisandbiologicalevaluationofflavonoidsasantiacetylcholinesteraseagent
AT amadfarediah synthesisandbiologicalevaluationofflavonoidsasantiacetylcholinesteraseagent