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 |
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| 5MG | 45 | In Stock |
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| 10MG | 76 | In Stock |
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| 25MG | 159 | In Stock |
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| 50MG | 231 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameS-Isocorydine(+)
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NoteResearch use only, not for human use.
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Brief DescriptionS-Isocorydine(+) and its derivatives have anticancer activities.
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DescriptionIsocorydine 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.
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In VitroIsocorydine (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.
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In VivoIsocorydine (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.
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SynonymsIsocorydine | Luteanin | d-Isocorydine | NSC32979
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number475-67-2
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Formula Weight341.41
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Molecular FormulaC20H23NO4
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 20 mg/mL (58.58 mM)
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SMILESCN1CCc2cc(c(c3c2[C@@H]1Cc1c3c(c(cc1)OC)O)OC)OC
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Chemical Name(S)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-11-ol
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Sun H, et al. PLoS One. 2012;7(5):e36808.
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