Eriocitrin

Eriocitrin

CAT N°: 25838
Price:

From 182.00 154.70

Eriocitrin is a flavonoid originally isolated from lemon peel that has antioxidant and enzyme inhibitory activity.{47241,47242,47243,47244,47245} Eriocitrin inhibits lipid peroxidation in a cell-free assay when used at a concentration of 10 µM and enhances the effect of ?-tocopherol (Item No. 25985) on lipid peroxidation.{47242} It also decreases thiobarbituric acid reactive substances (TBARS) in rat plasma when administered at a dose of 75 µmol/kg, indicating a reduction in lipid peroxidation.{47243} Eriocitrin prevents acute exercise-induced increases in TBARS, N?-(hexanoyl)lysine (HEL), o,o-dityrosine (DT), and nitrotyrosine (NT; Item No. 89540) in rat liver when administered at a dose of 600 mg/kg prior to exercise.{47244} It is also an inhibitor of monoamine oxidase A (MAO-A) and MAO-B (IC50s = 86.5 and 164 µM, respectively, for human recombinant receptors).{47245}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • (2S)-7-[[6-O-(6-deoxy-?-L-mannopyranosyl)-?-D-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-5-hydroxy-4H-1-benzopyran-4-one
  • Correlated keywords
    • 32737-63-6 52389-55-6 Flavanone T BARS HEL DT NT MAOA MAOB MA OB OA hexanoyl lysine o,odityrosine N?(hexanoyl)lysine Eriodictyol 7O-rutinoside 7-O 7? ?
  • Product Overview:
    Eriocitrin is a flavonoid originally isolated from lemon peel that has antioxidant and enzyme inhibitory activity.{47241,47242,47243,47244,47245} Eriocitrin inhibits lipid peroxidation in a cell-free assay when used at a concentration of 10 µM and enhances the effect of ?-tocopherol (Item No. 25985) on lipid peroxidation.{47242} It also decreases thiobarbituric acid reactive substances (TBARS) in rat plasma when administered at a dose of 75 µmol/kg, indicating a reduction in lipid peroxidation.{47243} Eriocitrin prevents acute exercise-induced increases in TBARS, N?-(hexanoyl)lysine (HEL), o,o-dityrosine (DT), and nitrotyrosine (NT; Item No. 89540) in rat liver when administered at a dose of 600 mg/kg prior to exercise.{47244} It is also an inhibitor of monoamine oxidase A (MAO-A) and MAO-B (IC50s = 86.5 and 164 µM, respectively, for human recombinant receptors).{47245}

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