Furnidipine

CAS No. 138661-03-7

Furnidipine( —— )

Catalog No. M36174 CAS No. 138661-03-7

Furnidipine significantly reduced AoD and AF and had antiarrhythmic and cardioprotective effects at low doses in a rat model.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 164 Get Quote
5MG 247 Get Quote
10MG 371 Get Quote
25MG 601 Get Quote
50MG 854 Get Quote
100MG 1134 Get Quote
500MG 2277 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Furnidipine
  • Note
    Research use only, not for human use.
  • Brief Description
    Furnidipine significantly reduced AoD and AF and had antiarrhythmic and cardioprotective effects at low doses in a rat model.
  • Description
    Furnidipine significantly reduced AoD and AF and had antiarrhythmic and cardioprotective effects at low doses in a rat model.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    138661-03-7
  • Formula Weight
    416.42
  • Molecular Formula
    C21H24N2O7
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    C(OCC1CCCO1)(=O)C=2C(C(C(OC)=O)=C(C)NC2C)C3=C(N(=O)=O)C=CC=C3
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • ML382

    ML382 is a potent and selective MrgX1 positive allosteric modulator(EC50 : 190 nM).ML382 enhances the ability of BAM8-22 to inhibit high-voltage-activated Ca2+ channels and attenuate spinal nociceptive transmission, both BAM8-22 and ML382 effectively attenuated evoked, persistent, and spontaneous pain without causing obvious side effects.?

  • D-(+)-Trehalose dihy...

    Trehalose is a natural alpha-linked disaccharide formed by an α,α-1,1-glucoside bond between two α-glucose units.

  • Calceolarioside B

    Calceolarioside B displays inhibition of aromatase. Calceolarioside B displays inhibition of human recombinant PKCalpha.