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Glaucine

CAS No. 475-81-0

Glaucine ( —— )

Catalog No. M21459 CAS No. 475-81-0

Glaucine has antitussive antioxidative potential and antiviral activities it may be an anti-arthritic agent it can enhance LPS and zymosan-induced IL-10 production. Glaucine can inhibit the migration and invasion of human breast cancer cells by MMP-9 inhibitory activity attenuating IκBα and NF-κB activities.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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10MG 132 In Stock
25MG 221 In Stock
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Biological Information

  • Product Name
    Glaucine
  • Note
    Research use only not for human use.
  • Brief Description
    Glaucine has antitussive antioxidative potential and antiviral activities it may be an anti-arthritic agent it can enhance LPS and zymosan-induced IL-10 production. Glaucine can inhibit the migration and invasion of human breast cancer cells by MMP-9 inhibitory activity attenuating IκBα and NF-κB activities.
  • Description
    Glaucine has antitussive antioxidative potential and antiviral activities it may be an anti-arthritic agent it can enhance LPS and zymosan-induced IL-10 production. Glaucine can inhibit the migration and invasion of human breast cancer cells by MMP-9 inhibitory activity attenuating IκBα and NF-κB activities.
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    475-81-0
  • Formula Weight
    355.4
  • Molecular Formula
    C21H25NO4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:30mg/ml(84.41mM)
  • SMILES
    CN(CC1)[C@@H](Cc(cc(c(OC)c2)OC)c2-c2c3OC)c2c1cc3OC
  • Chemical Name
    (6aS)-12910-Tetramethoxy-6-methyl-566a7-tetrahydro-4H-dibenzo[deg]quinoline

Shipping & Storage Information

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

Reference

1.Meyer G M J Meyer M R Wink C S D et al. Studies on the in vivo contribution of human cytochrome P450s to the hepatic metabolism of glaucine a new drug of abuse[J]. Biochemical Pharmacology 2013 86(10):1497-1506.
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