Home - Products - Metabolic Enzyme/Protease - P450 - Guan-fu base A hydrochloride(1394-48-5 free base)

Guan-fu base A hydrochloride(1394-48-5 free base)

CAS No. 618094-85-2

Guan-fu base A hydrochloride(1394-48-5 free base)( —— )

Catalog No. M24619 CAS No. 618094-85-2

Guan-fu base A hydrochloride is an antiarrhythmic alkaloid was isolated from Aconitum coreanum. Guanfu base A is hydrochloride a CYP2D6 inhibitor of human, monkey, and dog isoforms.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 155 In Stock
5MG 287 In Stock
10MG 430 In Stock
25MG 710 In Stock
50MG 977 In Stock
100MG 1321 In Stock
200MG Get Quote In Stock
500MG 2632 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Guan-fu base A hydrochloride(1394-48-5 free base)
  • Note
    Research use only, not for human use.
  • Brief Description
    Guan-fu base A hydrochloride is an antiarrhythmic alkaloid was isolated from Aconitum coreanum. Guanfu base A is hydrochloride a CYP2D6 inhibitor of human, monkey, and dog isoforms.
  • Description
    Guan-fu base A hydrochloride is an antiarrhythmic alkaloid was isolated from Aconitum coreanum. Guanfu base A is hydrochloride a CYP2D6 inhibitor of human, monkey, and dog isoforms.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    P450
  • Recptor
    CYP2D6
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    618094-85-2
  • Formula Weight
    ——
  • Molecular Formula
    ——
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ——
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Sun J , Peng Y , Wu H , et al. Guanfu base A, an antiarrhythmic alkaloid of Aconitum coreanum, Is a CYP2D6 inhibitor of human, monkey, and dog isoforms.[J]. Drug metabolism and disposition: the biological fate of chemicals, 2015, 43(5).
molnova catalog
related products
  • TMS

    TMS is a very selective and potent competitive inhibitor of P450 1B1 (CYP1A1). It has strong selectivity among P450 family 1 enzymes.

  • (-)-Sparteine sulfat...

    Sparteine is a class 1a antiarrhythmic agent; a sodium channel blocker. It is an alkaloid and can be extracted from scotch broom.

  • Ginsenoside Rg2

    Ginsenoside Rg2 is one of the major active components of ginseng, act as an NF-κB inhibitor.