S-Isocorydine(+)

CAS No. 475-67-2

S-Isocorydine(+)( Isocorydine | Luteanin | d-Isocorydine | NSC32979 )

Catalog No. M18591 CAS No. 475-67-2

S-Isocorydine(+) and its derivatives have anticancer activities.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 49 In Stock
5MG 45 In Stock
10MG 76 In Stock
25MG 159 In Stock
50MG 231 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
    S-Isocorydine(+)
  • Note
    Research use only, not for human use.
  • Brief Description
    S-Isocorydine(+) and its derivatives have anticancer activities.
  • Description
    Isocorydine is an alkaloid from root tubers of Stephania Kwangsiensis H.S. Lo.(In Vitro):Isocorydine (0-400 ug/ml; 48 hours) show a significant decrease in the IC50 for ICD and DOX, the CI values are 0.605, 0.644, 0.804, and 0.707 respectively for Huh-7, Hep-G2, SNU-449 and SNU-387.Isocorydine (0-400 ug/ml; 48 hours) abrogates DOX-induced upregulation of mesenchymal markers and the downregulation of epithelial markers in human HCC cell lines.(In Vivo):Isocorydine (intraperitoneal injection; 0.4 mg/kg; every 2 days for 2 weeks) retards the tumor growth, but the combined treatment of Doxorubicin (DOX) or ICD significantly inhibits tumor growth.
  • In Vitro
    Isocorydine (0-400 ug/ml; 48 hours) show a significant decrease in the IC50 for ICD and DOX, the CI values are 0.605, 0.644, 0.804, and 0.707 respectively for Huh-7, Hep-G2, SNU-449 and SNU-387. Isocorydine (0-400 ug/ml; 48 hours)abrogates DOX-induced upregulation of mesenchymal markers and the downregulation of epithelial markers in human HCC cell lines. Cell Viability Assay Cell Line:Huh-7, Hep-G2 , SNU-387, SNU-449 cells Concentration:0-400 ug/ml Incubation Time:24 hours Result:Had a higher cytotoxicity in HCC cells in comparison to ICD or DOX alone.Western Blot Analysis Cell Line:Huh-7, Hep-G2 , SNU-387, SNU-449 cells Concentration:Incubation Time:24 hours Result:Downregulated protein levels of Claundin-1 and E-cadherin.
  • In Vivo
    Isocorydine (intraperitoneal injection; 0.4 mg/kg; every 2 days for 2 weeks) retards the tumor growth, but the combined treatment of Doxorubicin (DOX) or ICD significantly inhibits tumor growth. Animal Model:Female nude mice Dosage:0.4 mg/ml Administration:Injected intraperitoneally every 2 days for 2 weeks Result:Combined treatment of isocorydine and DOX showed a promising potential to eradicate HCC.
  • Synonyms
    Isocorydine | Luteanin | d-Isocorydine | NSC32979
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    475-67-2
  • Formula Weight
    341.41
  • Molecular Formula
    C20H23NO4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 20 mg/mL (58.58 mM)
  • SMILES
    CN1CCc2cc(c(c3c2[C@@H]1Cc1c3c(c(cc1)OC)O)OC)OC
  • Chemical Name
    (S)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-11-ol

Shipping & Storage Information

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

Reference

1. Sun H, et al. PLoS One. 2012;7(5):e36808.
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