Matairesinoside

CAS No. 23202-85-9

Matairesinoside( —— )

Catalog No. M31574 CAS No. 23202-85-9

Matairesinoside is a natural product from Styrax japonica.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 211 In Stock
10MG 364 In Stock
25MG 600 In Stock
50MG 827 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Matairesinoside
  • Note
    Research use only, not for human use.
  • Brief Description
    Matairesinoside is a natural product from Styrax japonica.
  • Description
    Matairesinoside is a natural product from Styrax japonica.
  • In Vitro
    Matairesinoside shows high virus-cell fusion inhibitory activity with the fusion inhibition of 46.7%.Matairesinoside shows prominent free radical scavenging activity in the DPPH assay, with the IC50 is 2.19 μg/mL.Matairesinoside is most active against Pseudomonas aeruginosa (MIC of 0.001 mg/mL).
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    23202-85-9
  • Formula Weight
    520.53
  • Molecular Formula
    C26H32O11
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (192.11 mM)
  • SMILES
    ——
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • (Lys18)-Pseudin-2

    (Lys18)-Pseudin-2

  • XY101

    XY101 is a selective, metabolically stable and orally available agonist of RORγ inverse(IC50 of 30 nM and a Kd of 380 nM).

  • CALP1

    Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site; produces CaM-dependent activation of phosphodiesterase. Also binds to cytoplasmic sites on other Ca2+ channels, including NMDA and HIV-1 gp120-activated channels, inhibiting Ca2+-mediated cytotoxicity and apoptosis (IC50 = 52 μM). Shown to protect pancreatic acinar cells from gossypol induced necrosis. Inhibits VLA-5-mediated adhesion of mast cells to fibronectin in vitro and attenuates inflammatory cell influx in guinea pig lung in vivo.