Product overview

Name Isoguvacine hydrochloride
Purity >98%
Description Selective GABAA receptor agonist
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Biological Data

Biological description Selective GABAA receptor agonist (IC50 = 5.6 µM). Less potent than GABA. Shows anti-epileptic actions.

Solubility & Handling

Storage instructions Room temperature
Solubility overview Soluble in water (100mM)
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

Calculators

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Chemical Data

Purity >98%
Chemical name 1,2,3,6-Tetrahydro-4-pyridinecarboxylic acid hydrochloride
Molecular Weight 163.6
Chemical structure Isoguvacine hydrochloride  [68547-97-7] Chemical Structure
Molecular Formula C6H9NO2.HCl
CAS Number 68547-97-7
PubChem identifier 155107
SMILES C1CNCC=C1C(=O)O.Cl
InChi InChI=1S/C6H9NO2.ClH/c8-6(9)5-1-3-7-4-2-5;/h1,7H,2-4H2,(H,8,9);1H
InChiKey SUWREQRNTXCCBL-UHFFFAOYSA-N
MDL number MFCD00055192

References for Isoguvacine hydrochloride

References are publications that support the biological activity of the product
  • Effects of gamma-aminobutyric acid (GABA) agonists and a GABA uptake inhibitor on pharmacoresistant seizure like events in organotypic hippocampal slice cultures.

    Wahab A et al (2009) Epilepsy Res 86(2-3) : 113-23.
  • Understanding your inhibitions: effects of GABA and GABAA receptor modulation on brain cortical metabolism.

    Nasrallah FA et al (2009) J Neurochem 108(1) : 57-71.
  • Isoguvacine binding, uptake, and release: relation to the GABA system.

    White WF et al (1983) J Neurochem 40(6) : 1701-8.
  • Isoguvacine binding, uptake, and release: relation to the GABA system.

    White WF et al (1983) J Neurochem 40(6) : 1701-8.

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