Gabazine



Gabazine
Systematic (IUPAC) name
4-[6-imino-3-(4-methoxyphenyl)pyridazin-1-yl] butanoic acid hydrobromide
Identifiers
CAS number 104104-50-9
ATC code  ?
PubChem 107895
Chemical data
O3 
Mol. mass 368.226
Pharmacokinetic data
Bioavailability  ?
Metabolism  ?
Half life  ?
Excretion  ?
Therapeutic considerations
Pregnancy cat.

?

Legal status
Routes  ?

Gabazine (SR-95531) is a drug that acts as an receptors. It is used in scientific research and has no role in medicine, as it would be expected to produce convulsions if used in humans.[1]

Gabazine binds to the GABA recognition site of the receptor-channel complex and acts as an chloride flux across the cell membrane, and thus inhibiting neuronal depolarisation. While phasic (synaptic) inhibition is gabazine-sensitive, tonic (extrasynaptic) inhibition is gabazine-insensitive.[3]

References

  1. ^ Behrens CJ, van den Boom LP, Heinemann U. Effects of the GABA(A) receptor antagonists bicuculline and gabazine on stimulus-induced sharp wave-ripple complexes in adult rat hippocampus in vitro. European Journal of Neuroscience 2007 Apr;25(7):2170-81.
  2. ^ Ueno S, Bracamontes J, Zorumski C, Weiss DS, Steinbach JH. Bicuculline and gabazine are allosteric inhibitors of channel opening of the GABAA receptor. Journal of Neuroscience 1997 Jan 15;17(2):625-34.
  3. ^ Yeung JY, Canning KJ, Zhu G, Pennefather P, MacDonald JF, Orser BA. Tonically activated GABAA receptors in hippocampal neurons are high-affinity, low-conductance sensors for extracellular GABA. Molecular Pharmacology 2003 Jan;63(1):2-8.
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Gabazine". A list of authors is available in Wikipedia.