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Description
  • Coumarins have attracted intense interest in recent years because of their diverse pharmacological properties. According to our continuing investigations of biological effects of several coumarins, the structure-antioxidant activity relationships (SARs) of six naturally occurring coumarins and their 16 synthesized analogues were established. For this purpose, the very reliable colorimetric assay (ferric reducing antioxidant power) modified to be used in 96-well microplates was used. This approach, which determines the reducing capacity of tested compounds directly, has previously been used for the determination of SARs of flavonoids, but has not been used for SAR determination of coumarins. It is known that the biological properties and consequently, therapeutic application of simple coumarins depends upon the pattern of substitution. It was established that 7,8-dihydroxy- and 6,7-dihydroxy-4-methylcoumarins have shown excellent ferric-reducing properties.
  • Coumarins have attracted intense interest in recent years because of their diverse pharmacological properties. According to our continuing investigations of biological effects of several coumarins, the structure-antioxidant activity relationships (SARs) of six naturally occurring coumarins and their 16 synthesized analogues were established. For this purpose, the very reliable colorimetric assay (ferric reducing antioxidant power) modified to be used in 96-well microplates was used. This approach, which determines the reducing capacity of tested compounds directly, has previously been used for the determination of SARs of flavonoids, but has not been used for SAR determination of coumarins. It is known that the biological properties and consequently, therapeutic application of simple coumarins depends upon the pattern of substitution. It was established that 7,8-dihydroxy- and 6,7-dihydroxy-4-methylcoumarins have shown excellent ferric-reducing properties. (en)
Title
  • Evaluation of the antioxidant activity of several naturally occurring coumarins and their synthesized analogues by %22ferric reducing antioxidant power%22 assay
  • Evaluation of the antioxidant activity of several naturally occurring coumarins and their synthesized analogues by %22ferric reducing antioxidant power%22 assay (en)
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  • Evaluation of the antioxidant activity of several naturally occurring coumarins and their synthesized analogues by %22ferric reducing antioxidant power%22 assay
  • Evaluation of the antioxidant activity of several naturally occurring coumarins and their synthesized analogues by %22ferric reducing antioxidant power%22 assay (en)
skos:notation
  • RIV/00216208:11160/14:10281952!RIV15-MSM-11160___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • I, P(EE2.3.20.0235), S, V
http://linked.open...iv/cisloPeriodika
  • 1
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
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  • 15462
http://linked.open...ai/riv/idVysledku
  • RIV/00216208:11160/14:10281952
http://linked.open...riv/jazykVysledku
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  • structure-activity relationship; ferric reducing antioxidant power; coumarins; Antioxidant (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [4E38A89F140B]
http://linked.open...i/riv/nazevZdroje
  • Journal of Enzyme Inhibition and Medicinal Chemistry
http://linked.open...in/vavai/riv/obor
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http://linked.open...vavai/riv/projekt
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http://linked.open...v/svazekPeriodika
  • 29
http://linked.open...iv/tvurceVysledku
  • Kuča, Kamil
  • Cahlíková, Lucie
  • Jun, Daniel
  • Macáková, Kateřina
  • Opletal, Lubomír
  • Jahodář, Luděk
  • Řeháková, Zuzana
  • Kolečkář, Vít
http://linked.open...ain/vavai/riv/wos
  • 000330850300009
issn
  • 1475-6366
number of pages
http://bibframe.org/vocab/doi
  • 10.3109/14756366.2012.753589
http://localhost/t...ganizacniJednotka
  • 11160
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