Pinoresinol diglucoside

CAS No. 63902-38-5

Pinoresinol diglucoside( —— )

Catalog No. M18941 CAS No. 63902-38-5

Pinoresinol diglucoside is a putative α-glucosidase inhibiting compound. 2. Pinoresinol diglucoside is a important antihypertensive compound.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 65 In Stock
5MG 43 In Stock
10MG 77 In Stock
50MG 272 In Stock
100MG 494 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Pinoresinol diglucoside
  • Note
    Research use only, not for human use.
  • Brief Description
    Pinoresinol diglucoside is a putative α-glucosidase inhibiting compound. 2. Pinoresinol diglucoside is a important antihypertensive compound.
  • Description
    Pinoresinol diglucoside is a putative α-glucosidase inhibiting compound. Pinoresinol diglucoside is a important antihypertensive compound.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    α-glucosidase
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    63902-38-5
  • Formula Weight
    682.67
  • Molecular Formula
    C32H42O16
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (146.48 mM)
  • SMILES
    COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC6C(C(C(C(O6)CO)O)O)O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • Wnt agonist 1

    Wnt agonist 1 (BML-284) is a potent, selective and , cell-permeable Wnt signaling activator.

  • Deoxypodophyllotoxin...

    Isoanthricin ((Rac)-Deoxypodophyllotoxin) is the racemate of Deoxypodophyllotoxin. Deoxypodophyllotoxin is a potent antitumor and anti-inflammatory agent.

  • Fz7-21

    Fz7-21 is a peptide antagonist of FZD7 . It antagonises WNT3A-induced Wnt-β-catenin signalling in HEK293 expressing FZD7. Fz7-21 impairs Wnt/β-catenin signaling in HEK293 cells stimulated with exogenous WNT3A (IC50=100?nM) or transfected with a construct expressing WNT3A or WNT1. Fz7-21 also blocks WNT3A-mediated stabilization of β-catenin in mouse L cells (IC50=50?nM).