AMINOPYRIDINE - LATOXAN Technical Data Sheet
Back to Home Page


ION CHANNEL and RECEPTOR LIGANDS
TOXINS & ALKALOIDS

 
Google Custom Search


L9071 4-AMINOPYRIDINE
( 4-AP )

a weak non selective K+ channels blocker; convulsant; induces acetylcholine release; induces GABA neurons depolarization.

Pyridine derivative, C5H6N2, synthetic.


PRICES
QuantityUS DollarsEURO
5 g 37.80 27.00
25 g 151.20 108.00


  • Molecular Weight : 94.11 Da.

  • Melting Point : 155-158 °C.

  • Solubility in : soluble in water.

  • Purity min. : min. 97%.

  • Physical Form : white to tan solid.

  • Biological Activity : 10-4 - 10-5 M increases severalfold the release of acetylcholine from rat striatal slices superfused with an eserine-containing, choline-free medium, and causes stoichiometric decreases in the release of choline [3].

  • Toxicity (LD50) : rat (orally): 21 mg/kg; mice (orally): 19 mg/kg
    mice (i.v.): 7 mg/kg; rabbit (i.v.): 5.5 mg/kg
    rat (i.p.): 6.5 mg/kg; mice (i.p.): 10 mg/kg
    rat (s.c.): 19 mg/kg

  • Storage recommendations : store at room temperature.

  • Safety recommendations : very toxic.

  • CAS Reg. No. : 504-24-5

  • RTECS No. : US1750000

  • Bibliography :
    1. Rutecki P.A. et al., "4-Aminopyridine produces epileptiform activity in hippocampus and enhances synaptic excitation and inhibition." J. Neurophysiol. (1987). 57(6):1911-1924
    2. Ogata N. et al., "Differential inhibition of a transient K+ current by chlorpromazine and 4-aminopyridine in neurones of the rat dorsal root ganglia." Br. J. of Pharmacol. (1993). 109(4):1239-1246
    3. Buyukuysal R.L. et al., "4-Aminopyridine Increases Acetylcholine Release Without Diminishing Membrane Phosphatidylcholine." J. of Neurochem. (1990). 54(4):1302-1309
    4. Avoli M. et al., "4-Aminopyridine induces a long-lasting depolarizing GABA-ergic potential in human neocortical and hippocampal neurons maintained in vitro." Neurosci. Lett. (1988). 94(3):327-332
    5. Heemskerk F.M.J. et al., "4-Aminopyridine stimulates B-50 (GAP43) phosphorilation and [3H]Noradrenaline release in rat hippocampal slices." J. Neurochem. (1990). 54:863
    6. Robertson D.W. et al., "Potassium channel modulators: scientific applications and therapeutic promise." J. Med. Chem. (1990). 33(6):1529



    Latoxan - 20, Rue Léon Blum - F-26000 VALENCE - France
    Phone: +33.4.75.41.91.91 - Fax: +33.4.75.41.91.99
    contact@latoxan.com

    For Research Purposes Only - Not for Human Use.


    Revised : 26/04/2007 10:26 - Copyright © Latoxan