Fuziline

CAS No. 80665-72-1

Fuziline( —— )

Catalog No. M20295 CAS No. 80665-72-1

Fuziline shows significant insecticidal activity against Nilaparvata legen and Aphis medicagini. Fuziline shows activity against pentobarbital sodiuminduced cardiomyocytes damage by obviously recovering beating rhythm and increasing the cell viability.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 72 In Stock
2MG 35 In Stock
5MG 55 In Stock
10MG 89 In Stock
25MG 149 In Stock
50MG 216 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
    Fuziline
  • Note
    Research use only, not for human use.
  • Brief Description
    Fuziline shows significant insecticidal activity against Nilaparvata legen and Aphis medicagini. Fuziline shows activity against pentobarbital sodiuminduced cardiomyocytes damage by obviously recovering beating rhythm and increasing the cell viability.
  • Description
    Fuziline shows significant insecticidal activity against Nilaparvata legen and Aphis medicagini. Fuziline shows activity against pentobarbital sodiuminduced cardiomyocytes damage by obviously recovering beating rhythm and increasing the cell viability.
  • In Vitro
    Fuziline shows activity against pentobarbital sodiuminduced cardiomyocytes damage by obviously recovering beating rhythm and increasing the cell viability.
  • In Vivo
    Fuziline exhibits the mean half-life of 5.93 hours, 6.13 hours and 5.12?hours for 14?mg/kg, 2 4?mg/kg and 4?mg/kg, respectively, by oral administration in rat.
  • Synonyms
    ——
  • Pathway
    Microbiology/Virology
  • Target
    Antifection
  • Recptor
    Antifection
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    80665-72-1
  • Formula Weight
    453.6
  • Molecular Formula
    C24H39NO7
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (220.47 mM)
  • SMILES
    [H][C@]12C[C@]3([H])[C@]([H])([C@H]1O)[C@@](O)(C1[C@H](OC)[C@@]4([H])[C@]33[C@@H]1N(CC)C[C@]4(COC)CC[C@@H]3O)[C@@H](O)[C@@H]2OC
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Liang X Cheng P Xiao-Fang X et al. Alkaloids Isolated from the Lateral Root of Aconitum carmichaelii[J]. Molecules 2012 17(8):9939-9946.
molnova catalog
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