3',5,7-Trihydroxy-4'-methoxyflavanone, 97%
3',5,7-Trihydroxy-4'-methoxyflavanone, 97%
3',5,7-Trihydroxy-4'-methoxyflavanone, 97%
3',5,7-Trihydroxy-4'-methoxyflavanone, 97%
Thermo Scientific Chemicals

3',5,7-Trihydroxy-4'-methoxyflavanone, 97%

CAS: 520-33-2 | C16H14O6 | 302.28 g/mol
製品番号(カタログ番号) B20528.14
または、製品番号B20528-14
価格(JPY)
-
見積もりを依頼する
数量:
25 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS520-33-2
IUPAC Name(2S)-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one
Molecular FormulaC16H14O6
InChI KeyAIONOLUJZLIMTK-AWEZNQCLSA-N
SMILESCOC1=CC=C(C=C1O)[C@@H]1CC(=O)C2=C(O)C=C(O)C=C2O1
さらに表示
Appearance (Color)White to cream or pale yellow to pale brown
Identification (FTIR)Conforms
FormPowder
Assay (HPLC)≥96.0%
Melting Point (clear melt)225-236?C
(±)-Hesperetin is an antioxidant flavonoid. Induces G1-phase cell cycle arrest. Anti-inflammatory. (±)-Hesperetin suppresses NF-κB activation. Reduces cholesterol biosynthesis. Inhibits lipid peroxidation. Neuroprotective against neuronal oxidative damage.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(±)-Hesperetin is an antioxidant flavonoid. Induces G1-phase cell cycle arrest. Anti-inflammatory. (±)-Hesperetin suppresses NF-κB activation. Reduces cholesterol biosynthesis. Inhibits lipid peroxidation. Neuroprotective against neuronal oxidative damage.

Solubility
Soluble in water (partly), dilute alkalis, and ethanol (50 mg/ml).

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions. Keep away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. AA Hardigree.; JL Epler. Comparative mutagenesis of plant flavonoids in microbial systems. Mutation Research/Genetic Toxicology. 197858 (2-3), 1109-1114.
  2. LW Wattenberg.; MA Page.; JL Leong. Induction of increased benzpyrene hydroxylase activity by flavones and related compounds. Cancer Research. 196828 (1), 934-936.