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
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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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