Evaluation of the radical scavenging activity of a series of synthetic hydroxychalcones towards the DPPH radical

Sixteen hydroxychalcones were synthesized in sufficient purity by the Claisen–Schmidt condensation between appropriate acetophenones and aromatic aldehydes. All the compounds were evaluated for their ability to scavenge the stable free 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical. Important structur...

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Main Authors: STOYAN P. PARUSHEV, BISTRA A. STAMBOLIYSKA, DANIELA I. BATOVSKA, IVA T. TODOROVA
Format: Article
Language:English
Published: Serbian Chemical Society 2011-04-01
Series:Journal of the Serbian Chemical Society
Subjects:
Online Access:http://www.shd.org.rs/JSCS/Vol76/No4/02_4776_4135.pdf
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author STOYAN P. PARUSHEV
BISTRA A. STAMBOLIYSKA
DANIELA I. BATOVSKA
IVA T. TODOROVA
author_facet STOYAN P. PARUSHEV
BISTRA A. STAMBOLIYSKA
DANIELA I. BATOVSKA
IVA T. TODOROVA
author_sort STOYAN P. PARUSHEV
collection DOAJ
description Sixteen hydroxychalcones were synthesized in sufficient purity by the Claisen–Schmidt condensation between appropriate acetophenones and aromatic aldehydes. All the compounds were evaluated for their ability to scavenge the stable free 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical. Important structure–activity relationships were observed that strongly contribute to the knowledge for the design of DPPH radical scavenging chalcones. Relevant theoretical parameters were computed in an attempt to understand and explain the obtained experimental results.
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spelling doaj.art-20a7d7800d1d4faa964b02de56cdf7922022-12-21T21:19:45ZengSerbian Chemical SocietyJournal of the Serbian Chemical Society0352-51392011-04-01764491497Evaluation of the radical scavenging activity of a series of synthetic hydroxychalcones towards the DPPH radicalSTOYAN P. PARUSHEVBISTRA A. STAMBOLIYSKADANIELA I. BATOVSKAIVA T. TODOROVASixteen hydroxychalcones were synthesized in sufficient purity by the Claisen–Schmidt condensation between appropriate acetophenones and aromatic aldehydes. All the compounds were evaluated for their ability to scavenge the stable free 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical. Important structure–activity relationships were observed that strongly contribute to the knowledge for the design of DPPH radical scavenging chalcones. Relevant theoretical parameters were computed in an attempt to understand and explain the obtained experimental results.http://www.shd.org.rs/JSCS/Vol76/No4/02_4776_4135.pdfhydroxychalcones4’-chlorohydroxychalconessynthesisradical-scavenging activityDPPH free radical
spellingShingle STOYAN P. PARUSHEV
BISTRA A. STAMBOLIYSKA
DANIELA I. BATOVSKA
IVA T. TODOROVA
Evaluation of the radical scavenging activity of a series of synthetic hydroxychalcones towards the DPPH radical
Journal of the Serbian Chemical Society
hydroxychalcones
4’-chlorohydroxychalcones
synthesis
radical-scavenging activity
DPPH free radical
title Evaluation of the radical scavenging activity of a series of synthetic hydroxychalcones towards the DPPH radical
title_full Evaluation of the radical scavenging activity of a series of synthetic hydroxychalcones towards the DPPH radical
title_fullStr Evaluation of the radical scavenging activity of a series of synthetic hydroxychalcones towards the DPPH radical
title_full_unstemmed Evaluation of the radical scavenging activity of a series of synthetic hydroxychalcones towards the DPPH radical
title_short Evaluation of the radical scavenging activity of a series of synthetic hydroxychalcones towards the DPPH radical
title_sort evaluation of the radical scavenging activity of a series of synthetic hydroxychalcones towards the dpph radical
topic hydroxychalcones
4’-chlorohydroxychalcones
synthesis
radical-scavenging activity
DPPH free radical
url http://www.shd.org.rs/JSCS/Vol76/No4/02_4776_4135.pdf
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