Dihydromyricetin

CAS No. 27200-12-0

Dihydromyricetin( Ampelopsin | Ampeloptin )

Catalog No. M18341 CAS No. 27200-12-0

Dihydromyricetin is a potent inhibitor of dihydropyrimidinase with an IC50 of 48 μM. Dihydromyricetin can activate autophagy by inhibiting mTOR signaling.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 41 In Stock
5MG 37 In Stock
10MG 52 In Stock
25MG 69 In Stock
50MG 83 In Stock
100MG 129 In Stock
200MG Get Quote In Stock
500MG 322 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Dihydromyricetin
  • Note
    Research use only, not for human use.
  • Brief Description
    Dihydromyricetin is a potent inhibitor of dihydropyrimidinase with an IC50 of 48 μM. Dihydromyricetin can activate autophagy by inhibiting mTOR signaling.
  • Description
    Ampelopsin, also known as dihydromyricetin, is a type of flavonoid. It can be found in Cedrus deodara or in the Japanese raisin tree (Hovenia dulcis). It is also found in Erythrophleum africanum. The compound is credited with hepatoprotective effects observed in rodents. Use of Hovenia species in traditional Chinese herbal medicine as a hangover cure has led to research into the potential action of dihydromyricetin in counteracting the effects of alcohol in the brain.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Ampelopsin | Ampeloptin
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    GABAR
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    27200-12-0
  • Formula Weight
    320.25
  • Molecular Formula
    C15H12O8
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 100 mg/mL; 312.26 mM
  • SMILES
    C1=C(C=C(C(=C1O)O)O)[C@@H]2[C@H](C(=O)C3=C(C=C(C=C3O2)O)O)O
  • Chemical Name
    (2R,3R)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Zhang YS, et al. Yao Xue Xue Bao, 2003, 38(4), 241-244.
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