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Description
  • A series of diarylheptanoids, namely 1,7-bis-(3,4-dihydroxyphenyl)-heptan-3-one-5-O-D-xylopyranoside (oregonin), 1,7-bis-(3,4-dihydroxyphenyl)-3-hydroxyheptane-5-O-beta-D-xylopyranoside and 1,7-bis(4-hydroxyphenyl)-heptane-3-one-5-O-beta-D-glucopyranoside (platyphylloside), were isolated from the bark of alder family trees, a species widely spread over in Europe. As antioxidants, these natural polyphenols have a promising potential in various fields of application, but their redox reactivity is insufficiently characterized. In this work, their antioxidant activity is described using assays based on DPPH and ABTS(center dot+) radical scavenging, oxygen anion radicals (0) quenching. The standardized ORAC assay was also achieved, which measures the capacity to protect fluorescent molecules against oxidative degradation. The measured antioxidant activity was higher than that of the well-known antioxidant and biologically active diarylheptanoid curcumin. Molecular modeling was used to rationalize the differences in activity and the mechanisms of action. Thermodynamic descriptors mainly O-H bond dissociation enthalpies (BDEs) establish a clear structure-activity relationship.
  • A series of diarylheptanoids, namely 1,7-bis-(3,4-dihydroxyphenyl)-heptan-3-one-5-O-D-xylopyranoside (oregonin), 1,7-bis-(3,4-dihydroxyphenyl)-3-hydroxyheptane-5-O-beta-D-xylopyranoside and 1,7-bis(4-hydroxyphenyl)-heptane-3-one-5-O-beta-D-glucopyranoside (platyphylloside), were isolated from the bark of alder family trees, a species widely spread over in Europe. As antioxidants, these natural polyphenols have a promising potential in various fields of application, but their redox reactivity is insufficiently characterized. In this work, their antioxidant activity is described using assays based on DPPH and ABTS(center dot+) radical scavenging, oxygen anion radicals (0) quenching. The standardized ORAC assay was also achieved, which measures the capacity to protect fluorescent molecules against oxidative degradation. The measured antioxidant activity was higher than that of the well-known antioxidant and biologically active diarylheptanoid curcumin. Molecular modeling was used to rationalize the differences in activity and the mechanisms of action. Thermodynamic descriptors mainly O-H bond dissociation enthalpies (BDEs) establish a clear structure-activity relationship. (en)
Title
  • Elucidation of antioxidant properties of wood bark derived saturated diarylheptanoids: A comprehensive (DFT-supported) understanding
  • Elucidation of antioxidant properties of wood bark derived saturated diarylheptanoids: A comprehensive (DFT-supported) understanding (en)
skos:prefLabel
  • Elucidation of antioxidant properties of wood bark derived saturated diarylheptanoids: A comprehensive (DFT-supported) understanding
  • Elucidation of antioxidant properties of wood bark derived saturated diarylheptanoids: A comprehensive (DFT-supported) understanding (en)
skos:notation
  • RIV/61989592:15310/14:33152196!RIV15-MSM-15310___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(ED2.1.00/03.0058), P(EE2.3.20.0017), P(EE2.3.20.0058), P(GBP208/12/G016)
http://linked.open...iv/cisloPeriodika
  • JUL
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
  • Trouillas, Patrick
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 14360
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15310/14:33152196
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Structure-activity relationship; Electron transfer; Ionization potentials; O-H bond dissociation enthalpies; Molecular modeling; ORAC; Superoxide; ABTS(+); DPPH-; Antioxidants; Diarylheptanoids; Grey alder (Alnus incana) bark (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [EF3D8B066A1C]
http://linked.open...i/riv/nazevZdroje
  • Phytochemistry
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 103
http://linked.open...iv/tvurceVysledku
  • Martin, Nicolas
  • Trouillas, Patrick
  • Dizhbite, Tatyana
  • Krasilnikova, Jelena
  • Ponomarenko, Jevgenija
  • Telysheva, Galina
http://linked.open...ain/vavai/riv/wos
  • 000337777800022
issn
  • 0031-9422
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.phytochem.2014.03.010
http://localhost/t...ganizacniJednotka
  • 15310
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