Silybin

CAS No. 802918-57-6

Silybin( ——— )

Catalog No. M38664 CAS No. 802918-57-6

Silybin is a flavonolignan isolated from milk thistle (Silybum marianum) seeds. Silybin induces apoptosis and exhibits hepatoprotective, antioxidant, anti-inflammatory, anti-cancer activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 19 In Stock
25MG Get Quote In Stock
50MG Get Quote In Stock
100MG Get Quote In Stock

Biological Information

  • Product Name
    Silybin
  • Note
    Research use only, not for human use.
  • Brief Description
    Silybin is a flavonolignan isolated from milk thistle (Silybum marianum) seeds. Silybin induces apoptosis and exhibits hepatoprotective, antioxidant, anti-inflammatory, anti-cancer activity.
  • Description
    Silybin is a flavonolignan isolated from milk thistle (Silybum marianum) seeds. Silybin induces apoptosis and exhibits hepatoprotective, antioxidant, anti-inflammatory, anti-cancer activity.
  • In Vitro
    Silybin (0-200 mM; for 72 hours) has growth inhibition in a time- and dose-dependent manner. Silybin (68 μM; for 72 hours) induces apoptosis and increases the cells in G1-phase of ~22%. Silybin (68 μM; for 72 hours) induces AKT activity inhibition. Cell Viability Assay Cell Line:HepG2 cell growth Concentration:0-200 mM Incubation Time:For 72 hours Result:Had growth inhibition in a time- and dose-dependent manner with an IC50 of 68 μM.Apoptosis Analysis Cell Line:HepG2 cell growth Concentration: 68 μM;Incubation Time:For 72 hours Result:Induced apoptosis in a higher number of cells (60%) when compared to untreated cells.Cell Cycle Analysis Cell Line:HepG2 cell growth;Concentration:68 μM Incubation Time:For 72 hours Result:Increased the cells in G1-phase of ~22% and decreased of 47% the cells in S-phase.Western Blot Analysis Cell Line:HepG2 cell growth Concentration:68 μM Incubation Time:For 72 hours Result:Induced AKT activity inhibition.
  • In Vivo
    Silybin (50, 100?mg/kg/day; given intragastrically for the last 4 weeks) significantly lowers both serum and hepatic lipid accumulation. Animal Model:Male C57BL/6J mice (6-8 weeks old) with nonalcoholic fatty liver disease (NAFLD)Dosage:50, 100?mg/kg Administration:Given intragastrically; daily; for the last 4 weeks Result:Significantly lowered both serum and hepatic lipid accumulation.
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ———
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    802918-57-6
  • Formula Weight
    482.44
  • Molecular Formula
    C25H22O10
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 25 mg/mL (51.82 mM; ultraphonic; )
  • SMILES
    C(O)C1C(OC=2C(O1)=CC=C(C2)[C@H]3OC=4C(C(=O)[C@@H]3O)=C(O)C=C(O)C4)C5=CC(OC)=C(O)C=C5
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Silvia Zappavigna, et al. Silybin-Induced Apoptosis Occurs in Parallel to the Increase of Ceramides Synthesis and miRNAs Secretion in Human Hepatocarcinoma Cells. Int J Mol Sci. 2019 May 3;20(9):2190.?
molnova catalog
related products
  • Ademetionine disulfa...

    Ademetionine Disulfate Tosylate is the disulfate-tosylate mixed salt of a mixture of diastereoisomers of the ademetionine ions.

  • Ciprofloxacin EP IMp...

    Used as a new type of quinoline anti-bacterial drug ciprofloxacin intermediate.

  • PACAP (6-38), human,...

    PACAP (6-38), human, ovine, rat TFA is a potent PACAP receptor antagonist with IC50s of 30, 600, and 40 nM for PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2, respectively.