Euojaponine D

CAS No. 128397-42-2

Euojaponine D( ——— )

Catalog No. M38691 CAS No. 128397-42-2

Euojaponine D is a sesquiterpene alkaloids from Euonymus japonica (Celastraceae). Celastraceae has potent insecticidal activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 1832 Get Quote
25MG Get Quote Get Quote
50MG Get Quote Get Quote
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Euojaponine D
  • Note
    Research use only, not for human use.
  • Brief Description
    Euojaponine D is a sesquiterpene alkaloids from Euonymus japonica (Celastraceae). Celastraceae has potent insecticidal activity.
  • Description
    Euojaponine D is a natural product
  • In Vitro
    ———
  • In Vivo
    ———
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    128397-42-2
  • Formula Weight
    825.817
  • Molecular Formula
    C41H47NO17
  • Purity
    >98% (HPLC)
  • Solubility
    ———
  • SMILES
    ———
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Byung Hoon Han, et al. New Sesquiterpene Alkaloids from Euonymus japonica: Structures of Euojaponines D, F, J, and K. J. Nat. Prod. 1990, 53, 4, 909-914.
molnova catalog
related products
  • Cyperotundone

    Cyperotundone is a natural product from Cyperus rotundus.

  • Betamethasone disodi...

    Betamethasone disodium phosphate (Betamethasone 21-phosphate disodium salt) is a corticosteroid with anti-inflammatory properties that promotes the polarization of M1 to M2 macrophages by reducing the secretion of pro-inflammatory cytokines, and is utilized in research on keloids and rheumatoid arthritis.

  • γ-sanshool

    γ-Sanshool can be isolated from Zanthoxylum piperitum. γ-Sanshool inhibits human ACAT-1 and ACAT-2 activities with IC50s of 12.0 and 82.6 μM.