Pachycarpine

CAS No. 492-08-0

Pachycarpine( (+)-Sparteine )

Catalog No. M21189 CAS No. 492-08-0

Pachycarpine is a natural product extracted from scotch broom is a sodium channel blocker and a class 1a antiarrhythmic agent.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Pachycarpine
  • Note
    Research use only, not for human use.
  • Brief Description
    Pachycarpine is a natural product extracted from scotch broom is a sodium channel blocker and a class 1a antiarrhythmic agent.
  • Description
    Pachycarpine is a natural product extracted from scotch broom is a sodium channel blocker and a class 1a antiarrhythmic agent.(In Vitro):(+)-Sparteine (2 μM) reduces the ACh-induced current caused by activation of nicotinic AChRs in a voltage-independent manner. (+)-Sparteine (5, 10 μM) reduces the amplitude of the excitatory postsynaptic current (EPSC) and the time constant of the EPSC decay.
  • In Vitro
    (+)-Sparteine (2 μM) reduces the ACh-induced current caused by activation of nicotinic AChRs in a voltage-independent manner. (+)-Sparteine (5, 10 μM) reduces the amplitude of the excitatory postsynaptic current (EPSC) and the time constant of the EPSC decay.
  • In Vivo
    ——
  • Synonyms
    (+)-Sparteine
  • Pathway
    Endocrinology/Hormones
  • Target
    AChR
  • Recptor
    AChR
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    492-08-0
  • Formula Weight
    234.38
  • Molecular Formula
    C15H26N2
  • Purity
    >98% (HPLC)
  • Solubility
    H2O:2.86 mg/mL (12.20 mM; Need ultrasonic)
  • SMILES
    C1CCN2C[C@H]3C[C@H](CN4CCCC[C@H]34)[C@@H]2C1
  • Chemical Name
    (7R-(7alpha7aalpha14alpha14abeta))-Dodecahydro-714-methano-2H6H-dipyrido (12-a:1'2'-e)(15)diazocine

Shipping & Storage Information

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

Reference

1.Voitenko S et al. Effect of (+)-sparteine on nicotinic acetylcholine receptors in the neurons of rat superior cervical ganglion. Mol Pharmacol. 1991 Aug;40(2):180-5.
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