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γ-Acetylenic GABA hydrochloride (GAG hydrochloride)

Cat No.:V71848 Purity: ≥98%
γ-Acetylenic GABA (GAG) HCl is an irreversible GABA-aminase inhibitor.
γ-Acetylenic GABA hydrochloride (GAG hydrochloride)
γ-Acetylenic GABA hydrochloride (GAG hydrochloride) Chemical Structure CAS No.: 103451-26-9
Product category: GABA Receptor
This product is for research use only, not for human use. We do not sell to patients.
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Other Forms of γ-Acetylenic GABA hydrochloride (GAG hydrochloride):

  • γ-Acetylenic GABA (GAG)
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Product Description
γ-Acetylenic GABA (GAG) HCl is an irreversible GABA-aminase inhibitor. γ-Acetylenic GABA HCl can increase the concentration of GABA in the rat brain. γ-Acetylenic GABA ( HCl) is a click chemical reagent. It contains Alkyne groups and could undergo CuAAc (copper-catalyzed azide-alkyne cycloaddition reaction) with compounds bearing an Azide group.
γ-Acetylenic GABA hydrochloride (GAG hydrochloride) is an irreversible inhibitor of GABA-transaminase. It contains an alkyne group and is a click chemical reagent. γ-Acetylenic GABA hydrochloride can increase the concentration of GABA in the rat brain. It has a molecular weight of 163.60. The compound is used in neuroscience research to study GABAergic neurotransmission and neurological disorders.
Biological Activity I Assay Protocols (From Reference)
Targets
GABA-transaminase[1]
γ-Acetylenic GABA hydrochloride targets GABA-transaminase, the enzyme responsible for the degradation of GABA. By irreversibly inhibiting GABA-transaminase, the compound increases GABA levels in the brain. GABA is the chief inhibitory neurotransmitter in the central nervous system.
ln Vitro
In vitro activity data for γ-Acetylenic GABA hydrochloride show that it is an irreversible inhibitor of GABA-transaminase. The compound inhibits GABA-transaminase activity. It is a click chemical reagent due to the presence of an alkyne group.
ln Vivo
γ-Acetylenic GABA hydrochloride (100 mg/kg ip) increases the amount of GABA in the rat brain several times over and inhibits GABA-transaminase activity[2].
γ-Acetylenic GABA hydrochloride (100 mg/kg i.p.) inhibits GABA-transaminase activity and causes a several-fold increase in the concentration of GABA in rat brain. This in vivo activity demonstrates the compound's efficacy in raising brain GABA levels.
Enzyme Assay
The in vitro enzyme assay for γ-Acetylenic GABA hydrochloride involves measuring its inhibition of GABA-transaminase activity. Recombinant GABA transaminase is incubated with GABA as a substrate. The production of succinic semialdehyde is monitored. γ-Acetylenic GABA hydrochloride is incubated with the enzyme and substrate at various concentrations. The IC50 value is determined by fitting the inhibition data to a dose-response curve.
Cell Assay
In vitro cellular assays for γ-Acetylenic GABA hydrochloride typically use neuronal cell lines to assess its effects on GABA levels. Cells are treated with the compound at various concentrations. GABA levels in the cell lysate or medium are measured using HPLC or ELISA.
Animal Protocol
γ-Acetylenic GABA hydrochloride has been used in vivo in animal models. At 100 mg/kg i.p., it inhibits GABA-transaminase activity and causes a several-fold increase in GABA concentration in rat brain. The compound has been studied in the context of tardive dyskinesia.
ADME/Pharmacokinetics
Pharmacokinetic properties of γ-Acetylenic GABA hydrochloride are not extensively documented. As a small molecule with a molecular weight of 163.60, the compound is expected to have reasonable bioavailability. Its alkyne group may influence its metabolism. Further pharmacokinetic studies are necessary to fully characterize its PK profile.
Toxicity/Toxicokinetics
Toxicological data for γ-Acetylenic GABA hydrochloride are not extensively available in the public domain. As a research compound, it has not undergone extensive toxicological evaluation. Standard cytotoxicity assays in cell lines may have been performed to assess safety margins. Further preclinical toxicology studies would be required before clinical development.
References

[1]. gamma-Acetylenic GABA in tardive dyskinesia. Arch Gen Psychiatry. 1980 Dec;37(12):1376-9.

[2]. The effect of gamma-acetylenic GABA, an enzyme-activated irreversible inhibitor of GABA-transaminase, on dopamine pathways of the extrapyramidal and limbic systems. Eur J Pharmacol. 1978 Aug 15;50(4):325-36.

[3]. Gamma-aminobutyric acid agonists for neuroleptic-induced tardive dyskinesia. Cochrane Database Syst Rev. 2011 Apr 13;(4):CD000203.

Additional Infomation
γ-Acetylenic GABA hydrochloride (GAG hydrochloride) is an irreversible inhibitor of GABA-transaminase. It increases GABA concentration in rat brain. The compound has a molecular weight of 163.60. No clinical trials or regulatory approvals have been reported.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Physicochemical Properties
Molecular Formula
C6H10CLNO2
Molecular Weight
163.60
Exact Mass
163.04
CAS #
103451-26-9
Related CAS #
γ-Acetylenic GABA; 57659-38-8
PubChem CID
86740723
Appearance
White to light yellow solid powder
Hydrogen Bond Donor Count
3
Rotatable Bond Count
3
Heavy Atom Count
10
Complexity
144
Defined Atom Stereocenter Count
0
SMILES
C#CC(CCC(=O)O)N.Cl
InChi Key
ZAVKUGNSMAPIEF-UHFFFAOYSA-N
InChi Code
InChI=1S/C6H9NO2.ClH/c1-2-5(7)3-4-6(8)9;/h1,5H,3-4,7H2,(H,8,9);1H
Chemical Name
4-aminohex-5-ynoic acid;hydrochloride
HS Tariff Code
2934.99.9001
Storage

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

Note: Please store this product in a sealed and protected environment, avoid exposure to moisture.
Shipping Condition
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
Solubility Data
Solubility (In Vitro)
DMSO: ~200 mg/mL (~1222.5 mM; with ultrasonication)
Solubility (In Vivo)
Solubility in Formulation 1: ≥ 5 mg/mL (30.56 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), Clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of DMSO stock solution (50.0 mg/mL) to 900 μL of 20% SBE-β-CD saline and mix well.
Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 6.1125 mL 30.5623 mL 61.1247 mL
5 mM 1.2225 mL 6.1125 mL 12.2249 mL
10 mM 0.6112 mL 3.0562 mL 6.1125 mL

*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.

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Note: Chemical formula is case sensitive: C12H18N3O4  c12h18n3o4
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In vivo Formulation Calculator (Clear solution)
Step 1: Enter information below (Recommended: An additional animal to make allowance for loss during the experiment)
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Calculation results

Working concentration: mg/mL;

Method for preparing DMSO stock solution: mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.

Method for preparing in vivo formulation::Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O,mix and clarify.

(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
             (2) Be sure to add the solvent(s) in order.

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