Fangchinoline

CAS No. 436-77-1

Fangchinoline( —— )

Catalog No. M17509 CAS No. 436-77-1

Fangchinoline is extracted from Stephania tetrandra S. Moore.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 39 Get Quote
10MG 56 Get Quote
25MG 87 Get Quote
50MG 133 Get Quote
100MG 200 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Fangchinoline
  • Note
    Research use only, not for human use.
  • Brief Description
    Fangchinoline is extracted from Stephania tetrandra S. Moore.
  • Description
    Fangchinoline is extracted from Stephania tetrandra S. Moore.(In Vitro):Fangchinoline (2.5-40 μM; 24-96 hours) inhibits both T24 and 5637 cells in dose-dependent manner, the IC50 values of Fangchinoline in T24 cells are 19.0 μM (24 h), 12.0 μM (48 h) and 7.57 μM (72 h), and 11.9 μM (24 h), 9.92 μM (48 h) and 7.13 μM (72 h) in 5637 cells.Fangchinoline (5 μM; 24 hours) induces a significant increase in the LC3-II/LC3-I ratio and a decrease in p62 in both T24 and 5637 cells, and causes a significant increase in the cleavage of caspase-3.
  • In Vitro
    Fangchinoline (2.5-40 μM; 24-96 hours) inhibits both T24 and 5637 cells in dose-dependent manner, the IC50 values of Fangchinoline in T24 cells are 19.0 μM (24 h), 12.0 μM (48 h) and 7.57 μM (72 h), and 11.9 μM (24 h), 9.92 μM (48 h) and 7.13 μM (72 h) in 5637 cells.Fangchinoline (5 μM; 24 hours) induces a significant increase in the LC3-II/LC3-I ratio and a decrease in p62 in both T24 and 5637 cells, and causes a significant increase in the cleavage of caspase-3. Cell Viability AssayCell Line:T24 and 5637 cells Concentration:2.5 μM; 5 μM; 10 μM; 20 μM; 30 μM; 40 μM Incubation Time:24 hours; 48 hours; 96 hours Result:Inhibited both T24 and 5637 cells proliferation.Western Blot Analysis Cell Line:T24 and 5637 cells Concentration:5 μM Incubation Time:24 hours Result:Incresed LC3-II/LC3-I ratio and the cleavage of caspase-3.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Neuroscience
  • Target
    GluR
  • Recptor
    FAK
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    436-77-1
  • Formula Weight
    608.72
  • Molecular Formula
    C37H40N2O6
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (82.14 mM)
  • SMILES
    O1c2c3[C@@H](N(CCc3cc(OC)c2O)C)Cc2cc(Oc3ccc(C[C@@H]4N(CCc5c4cc1c(OC)c5)C)cc3)c(OC)cc2
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Guo B, et al. J Drug Target. 2015 Apr;23(3):266-74.
molnova catalog
related products
  • KML29

    KML29 is highly selective and effective monoacylglycerol lipase (MAGL) inhibitor.

  • VU 0469650

    VU 0469650 is a potent and selective negative allosteric modulator of mGluR1 (IC50 = 99 nM).

  • (R)-ADX-47273

    (R)-ADX-47273 is a potent mGluR5 positive allosteric modulator(EC50 of 168 nM for potentiation ).