Reynoutrin

CAS No. 549-32-6

Reynoutrin( Quercetin-3-D-xyloside | Reinutrin )

Catalog No. M21060 CAS No. 549-32-6

Reynoutrin with antioxidant and radical-scavenging activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 136 In Stock
5MG 122 In Stock
10MG 183 In Stock
25MG 307 In Stock
50MG 445 In Stock
100MG 638 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Reynoutrin
  • Note
    Research use only, not for human use.
  • Brief Description
    Reynoutrin with antioxidant and radical-scavenging activity.
  • Description
    Reynoutrin with antioxidant and radical-scavenging activity.
  • In Vitro
    Reynoutrin shows potent antioxidant activity, with pEC50 of 5.37 against fluorescein oxidation.
  • In Vivo
    ——
  • Synonyms
    Quercetin-3-D-xyloside | Reinutrin
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    549-32-6
  • Formula Weight
    434.35
  • Molecular Formula
    C20H18O11
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:150 mg/mL (345.34 mM)
  • SMILES
    O=c1c(O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)c(-c2ccc(O)c(O)c2)oc2cc(O)cc(O)c12
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Ho R Violette et al. Antioxidant potential and radical-scavenging effects of flavonoids from the leaves of Psidium cattleianum grown in French Polynesia[J]. Natural Product Research 2012.
molnova catalog
related products
  • Dimethylmatairesinol

    Dimethylmatairesinol (compound 8) is a lignan compound isolated from the seed of Hernandia nymphaeifolia. Dimethylmatairesinol shows cytotoxicity against the KKU-M156 and HepG2 cell line with IC50s of 5.4 μM (Emax 59%) and 5.2 μM (Emax 78%), respectively.

  • CB-TH

    CB-TH

  • DCZ0415

    DCZ0415 induces antimyeloma activity in vitro, in vivo and in primary cells of drug-resistant myeloma patients. DCZ0415 is a potent TRIP13 inhibitor that can impair the repair of non-homologous end junctions and inhibit NF-κB activity.DCZ0415 (10, 20 μM; 72 hours) showed a marked reduction in colony formation, indicating that it inhibited cell proliferation.