CAS 68547-97-7|Isoguvacine Hydrochloride

Introduction:Basic information about CAS 68547-97-7|Isoguvacine Hydrochloride, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameIsoguvacine Hydrochloride
CAS Number68547-97-7Molecular Weight163.60200
Density/Boiling Point/
Molecular FormulaC6H10ClNO2Melting Point/
MSDSUSAFlash Point/
Symbol
GHS07
Signal WordWarning

Names

Name1,2,3,6-Tetrahydro-4-pyridinecarboxylic Acid Hydrochloride
SynonymMore Synonyms

Isoguvacine Hydrochloride BiologicalActivity

DescriptionIsoguvacine hydrochloride is a GABA receptor agonist.
Related CatalogSignaling Pathways >>Membrane Transporter/Ion Channel >>GABA ReceptorSignaling Pathways >>Neuronal Signaling >>GABA ReceptorResearch Areas >>Neurological Disease
Target

GABA[1]

In VitroIsoguvacine binds to a mouse forebrain synaptic membrane preparation. The specific binding is displaceable by GABA, muscimol and bicuculline but not by picrotoxin or diaminobutyric acid. Kinetic data suggest two binding affinities. Highest levels of binding are observed in the cerebellum, cortex and hippocampus[1]. Isoguvacine binds to membrane preparations of rat forebrain with pharmacological characteristics similar to the postsynaptic GABA recognition site: that it is transported into synaptosomal preparations by an uptake system similar to the high-affinity GABA uptake system; and that recently accumulated isoguvacine is released in a Ca2+-dependent manner and by heteroexchange with external GABA[2]. Isoguvacine at a concentration of 50 μM blocks the seizure like events in 2 out of 6 organotypic hippocampal slice cultures. Isoguvacine inhibits the low magnesium induced seizure like events dose dependently[3].
Kinase AssayThe assay for 3H-Isoguvacine binding is carried out as follows: membranes suspended in Tris-citrate buffer pH 7.1 are incubated at 4°C for 10 min with 8 nM 3H-Isoguvacine. Identical samples are incubated in the presence of cold 0.5 mM GABA or 10 μM cold isoguvacine. The assay is terminated by centrifugation for 10 min at 4°C in a micro-centrifuge. The supernatants are rapidly aspirated and the surface of the pellets washed (2x) with ice-cold buffer. The pellet is resuspended in I00 μL of 0.1% Triton and placed in a scintillation vial. The assay tube is washed with I00 μL of distilled water and the wash added to the vial along with 10 ml of PCS: xylene (2:1). Counting efficiency is determined to be 40-45% in a Beckman liquid scintillation counter. Specific binding is defined as those radioactive cpm of bound 3H-Isoguvacine that are displaced by excess cold isoguvacine or GABA[1].
References

[1]. Morin AM, et al. The binding of 3H-isoguvacine to mouse brain synapticmembranes. Life Sci. 1980 Apr 14;26(15):1239-45.

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

[3]. Wahab A, et al. Effects of gamma-aminobutyric acid (GABA) agonists and a GABA uptake inhibitor on pharmacoresistant seizure like events in organotypic hippocampal slice cultures. Epilepsy Res. 2009 Oct;86(2-3):113-23.

Chemical & Physical Properties

Molecular FormulaC6H10ClNO2
Molecular Weight163.60200
Exact Mass163.04000
PSA49.33000
LogP1.12150
InChIKeySUWREQRNTXCCBL-UHFFFAOYSA-N
SMILESCl.O=C(O)C1=CCNCC1

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH315-H319-H335
Precautionary StatementsP261-P305 + P351 + P338
Personal Protective Equipmentdust mask type N95 (US);Eyeshields;Gloves
Hazard CodesXi
RIDADRNONH for all modes of transport

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Synonyms

1,2,3,6-tetrahydropyridine-4-carboxylic acid,hydrochloride
Isoguvacine (hydrochloride)
Isoguvacine Hydrochloride
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