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  3. γ-Aminobutyric acid

γ-Aminobutyric acid  (Synonyms: 4-Aminobutyric acid)

Cat. No.: HY-N0067 Purity: 99.71%
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γ-Aminobutyric acid (4-Aminobutyric acid) is a major inhibitory neurotransmitter in the adult mammalian brain, binding to the ionotropic GABA receptors (GABAA receptors) and metabotropic receptors (GABAB receptors. γ-Aminobutyric acid shows calming effect by blocking specific signals of central nervous system.

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CAS No. : 56-12-2

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Customer Review

Based on 5 publication(s) in Google Scholar

Other Forms of γ-Aminobutyric acid:

Top Publications Citing Use of Products
Bio/Physico-chemical Assay
In Vivo Efficacy Study
Histological Imaging/Staining
WB
Flow Cytometry

    γ-Aminobutyric acid purchased from MedChemExpress. Usage Cited in: Adv Sci (Weinh). 2025 Jul 12:e09440.  [Abstract]

    γ-Aminobutyric acid (120 s).Intracellular calcium release induced by rac-BHFF in HEK293 cells co-transfected with the indicated constructs in the presence of EC20 of GABA was observed.

    γ-Aminobutyric acid purchased from MedChemExpress. Usage Cited in: Life Sci. 2023 Mar 15:317:121439.  [Abstract]

    Macroscopic images of mice on day 21 of the experiment, the time by which mice treated with CRS showed hair growth inhibition compared to control. Mice treated with CRS and γ-Aminobutyric acid (100 mM) showed aggravation of hair growth inhibition, whereas mice treated with CRS and picrotoxin exhibited more hair patches on the dorsal skin than those in the CRS group.

    γ-Aminobutyric acid purchased from MedChemExpress. Usage Cited in: Life Sci. 2023 Mar 15:317:121439.  [Abstract]

    γ-Aminobutyric acid was dissolved in H₂O to a final concentration of 100 mM. H&E staining showed representative histological changes in the hair follicles, and the image of Ki67 staining in the back skin tissues was obtained.

    γ-Aminobutyric acid purchased from MedChemExpress. Usage Cited in: Life Sci. 2023 Mar 15:317:121439.  [Abstract]

    Western blot showing CCND1 levels in DP cells treated with 100 μM γ-aminobutyric acid for 0, 24, or 48 h.

    γ-Aminobutyric acid purchased from MedChemExpress. Usage Cited in: Life Sci. 2023 Mar 15:317:121439.  [Abstract]

    Cell distribution in the cell cycle G1, S, and G2 phases after treatment with γ-aminobutyric acid for 48 h at a concentration gradient was analyzed.

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    Description

    γ-Aminobutyric acid (4-Aminobutyric acid) is a major inhibitory neurotransmitter in the adult mammalian brain, binding to the ionotropic GABA receptors (GABAA receptors) and metabotropic receptors (GABAB receptors. γ-Aminobutyric acid shows calming effect by blocking specific signals of central nervous system[1][2].

    IC50 & Target

    Microbial Metabolite

     

    Human Endogenous Metabolite

     

    Cellular Effect
    Cell Line Type Value Description References
    HEK293 EC50
    0.43 μM
    Compound: GABA
    Antagonist activity at human rho1 GABAc receptor in HEK293 cells by FMP assay
    Antagonist activity at human rho1 GABAc receptor in HEK293 cells by FMP assay
    [PMID: 17722904]
    HEK293 EC50
    0.53 μM
    Compound: GABA
    Agonist activity at human GABA-B B1/B2 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated cAMP accumulation after 3 hrs by luciferase reporter gene assay
    Agonist activity at human GABA-B B1/B2 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated cAMP accumulation after 3 hrs by luciferase reporter gene assay
    [PMID: 23428109]
    HEK293 EC50
    0.55 μM
    Compound: GABA
    Agonist activity at human GABAC rho 1 receptor expressed in HEK293 cells by FMP assay
    Agonist activity at human GABAC rho 1 receptor expressed in HEK293 cells by FMP assay
    [PMID: 17655213]
    HEK293 EC50
    12.8 μM
    Compound: GABA
    Agonist activity at rat GABA alpha-1-T129S-beta-2-gamma-2 receptor mutant expressed in HEK293 cells by Whole-cell patch-clamp technique
    Agonist activity at rat GABA alpha-1-T129S-beta-2-gamma-2 receptor mutant expressed in HEK293 cells by Whole-cell patch-clamp technique
    [PMID: 17655213]
    HEK293 EC50
    354 μM
    Compound: 119
    Substrate uptake by the Taurine Transporter (TauT, SLC6A6) as assessed by the fluorescent FLIPR membrane potential dye in HEK-293 JumpIN-SLC6A6 cells (PubChem AID: 1794824)
    Substrate uptake by the Taurine Transporter (TauT, SLC6A6) as assessed by the fluorescent FLIPR membrane potential dye in HEK-293 JumpIN-SLC6A6 cells (PubChem AID: 1794824)
    10.5281/zenodo.7360560
    HEK293 EC50
    36 μM
    Compound: 119
    Substrate uptake by the Sodium- and Chloride-Dependent BetaineTransporter (BGT-1, SLC6A12) as assessed by the fluorescent FLIPR membrane potential dye in HEK-293 JumpIN-SLC6A12 cells (PubChem AID: 1794822)
    Substrate uptake by the Sodium- and Chloride-Dependent BetaineTransporter (BGT-1, SLC6A12) as assessed by the fluorescent FLIPR membrane potential dye in HEK-293 JumpIN-SLC6A12 cells (PubChem AID: 1794822)
    10.5281/zenodo.7360527
    HEK293 EC50
    43 μM
    Compound: GABA
    Agonist activity at GABA alpha-1-beta-2-gamma-2 receptor expressed in HEK293 cells by Whole-cell patch-clamp technique
    Agonist activity at GABA alpha-1-beta-2-gamma-2 receptor expressed in HEK293 cells by Whole-cell patch-clamp technique
    [PMID: 17655213]
    HEK293 EC50
    6 μM
    Compound: GABA
    Agonist activity at human GABAC rho 1 receptor expressed in HEK293 cells by Whole-cell patch-clamp technique
    Agonist activity at human GABAC rho 1 receptor expressed in HEK293 cells by Whole-cell patch-clamp technique
    [PMID: 17655213]
    HEK293 IC50
    5 μM
    Compound: 1, GABA
    Inhibition of [3H]GABA uptake at mouse GAT1 expressed in HEK293 cells after 25 mins by scintillation counting analysis
    Inhibition of [3H]GABA uptake at mouse GAT1 expressed in HEK293 cells after 25 mins by scintillation counting analysis
    [PMID: 23336362]
    IMR-32 EC50
    2.94 μM
    Compound: GABA
    Agonist activity at GABA type-A receptor in human IMR32 cells after 2 hrs by Epic DMR assay
    Agonist activity at GABA type-A receptor in human IMR32 cells after 2 hrs by Epic DMR assay
    10.1039/C5MD00442J
    Oocyte EC50
    0.8 μM
    Compound: 1, GABA
    Agonist activity at human GABAc Rho1 receptor expressed in Xenopus oocytes assessed as whole cell current production by two electrode voltage clamp method
    Agonist activity at human GABAc Rho1 receptor expressed in Xenopus oocytes assessed as whole cell current production by two electrode voltage clamp method
    [PMID: 18528996]
    Oocyte EC50
    0.99 μM
    Compound: GABA
    Agonist activity at human alpha1beta2gamma2L GABAA receptor expressed in Xenopus oocytes assessed as potentiation of channel current response by two-electrode voltage clamp electrophysiology assay
    Agonist activity at human alpha1beta2gamma2L GABAA receptor expressed in Xenopus oocytes assessed as potentiation of channel current response by two-electrode voltage clamp electrophysiology assay
    [PMID: 22029276]
    Oocyte EC50
    1.19 μM
    Compound: GABA
    Agonist activity at human recombinant GABAc rho1 receptor expressed in Xenopus laevis oocytes at -60mV by two-electrode voltage clamp method
    Agonist activity at human recombinant GABAc rho1 receptor expressed in Xenopus laevis oocytes at -60mV by two-electrode voltage clamp method
    [PMID: 17981464]
    Oocyte EC50
    1.7 μM
    Compound: 1, GABA
    Agonist activity at human GABAb 1A/2 receptor expressed in Xenopus oocytes assessed as whole cell current production by two electrode voltage clamp method
    Agonist activity at human GABAb 1A/2 receptor expressed in Xenopus oocytes assessed as whole cell current production by two electrode voltage clamp method
    [PMID: 18528996]
    Oocyte EC50
    10 μM
    Compound: GABA
    Activity at rat wild type GABAA alpha-1-beta-2 receptor expressed in Xenopus laevis oocytes at -60 mV by Two-Electrode voltage clamp method
    Activity at rat wild type GABAA alpha-1-beta-2 receptor expressed in Xenopus laevis oocytes at -60 mV by Two-Electrode voltage clamp method
    [PMID: 18651727]
    Oocyte EC50
    136 μM
    Compound: GABA
    Activity at rat GABAA alpha-1T129C-beta-2 receptor mutant expressed in Xenopus laevis oocytes at -60 mV by Two-Electrode voltage clamp method
    Activity at rat GABAA alpha-1T129C-beta-2 receptor mutant expressed in Xenopus laevis oocytes at -60 mV by Two-Electrode voltage clamp method
    [PMID: 18651727]
    Oocyte EC50
    21.1 μM
    Compound: 1, GABA
    Agonist activity at human alpha-1-beta-2-gamma-2L GABAA receptor expressed in Xenopus oocytes assessed as inhibition of current production by two electrode voltage clamp method
    Agonist activity at human alpha-1-beta-2-gamma-2L GABAA receptor expressed in Xenopus oocytes assessed as inhibition of current production by two electrode voltage clamp method
    [PMID: 18528996]
    Oocyte EC50
    28 μM
    Compound: GABA
    Agonist activity on human Gamma-aminobutyric acid A receptor alpha-3-beta-3-gamma-2 expressed in Xenopus oocytes
    Agonist activity on human Gamma-aminobutyric acid A receptor alpha-3-beta-3-gamma-2 expressed in Xenopus oocytes
    [PMID: 11412984]
    Oocyte EC50
    3 μM
    Compound: GABA
    Effective agonist dose for human Gamma-aminobutyric acid A receptor alpha-5-beta-3-gamma-2 expressed in Xenopus oocytes
    Effective agonist dose for human Gamma-aminobutyric acid A receptor alpha-5-beta-3-gamma-2 expressed in Xenopus oocytes
    [PMID: 11412984]
    Oocyte EC50
    40 μM
    Compound: GABA
    Agonist activity on human Gamma-aminobutyric acid A receptor alpha-2-beta-3-gamma-2 expressed in Xenopus oocytes
    Agonist activity on human Gamma-aminobutyric acid A receptor alpha-2-beta-3-gamma-2 expressed in Xenopus oocytes
    [PMID: 11412984]
    Oocyte EC50
    430 μM
    Compound: GABA
    Activity at rat GABAA alpha-1F64C-beta-2 receptor mutant expressed in Xenopus laevis oocytes at -60 mV by Two-Electrode voltage clamp method
    Activity at rat GABAA alpha-1F64C-beta-2 receptor mutant expressed in Xenopus laevis oocytes at -60 mV by Two-Electrode voltage clamp method
    [PMID: 18651727]
    Oocyte EC50
    5540 μM
    Compound: GABA
    Activity at rat GABAA alpha-1R66C-beta-2 receptor mutant expressed in Xenopus laevis oocytes at -60 mV by Two-Electrode voltage clamp method
    Activity at rat GABAA alpha-1R66C-beta-2 receptor mutant expressed in Xenopus laevis oocytes at -60 mV by Two-Electrode voltage clamp method
    [PMID: 18651727]
    Oocyte EC50
    6.5 μM
    Compound: GABA
    Activity at rat GABAA alpha-1S68C-beta-2 receptor mutant expressed in Xenopus laevis oocytes at -60 mV by Two-Electrode voltage clamp method
    Activity at rat GABAA alpha-1S68C-beta-2 receptor mutant expressed in Xenopus laevis oocytes at -60 mV by Two-Electrode voltage clamp method
    [PMID: 18651727]
    Oocyte EC50
    80 μM
    Compound: GABA
    Effective agonist dose for human Gamma-aminobutyric acid A receptor alpha-1-beta-3-gamma-2 expressed in Xenopus oocytes
    Effective agonist dose for human Gamma-aminobutyric acid A receptor alpha-1-beta-3-gamma-2 expressed in Xenopus oocytes
    [PMID: 11412984]
    In Vitro

    γ-Aminobutyric acid (30 μM) depolarizes cortical progenitor cells (E16 cells), results an inward current in ventricular zone (VZ) cells, and induces DNA synthesis inhibition, with half-maximal response concentration of 5 μM[3].
    Cortical plate (cp) neurons expresses glutamic acid decarboxylase (GAD), γ-Aminobutyric acid (1-5 μM; 18 h) stimulates the motility and arrests the migration of cp cells, while the chemotropic signal is involved G-protein activation[4].
    γ-Aminobutyric acid activates GABA A receptors, causing cell cycle arrest in S phase and limiting growth[5].

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    Cell Migration Assay [4]

    Cell Line: Cortical plate (cp) neurons
    Concentration: 1-5 μM
    Incubation Time: 18 hours
    Result: Promoted motility via G-protein activation and arrested attractantinduced migration via GABAA receptor-mediated depolarization.
    In Vivo

    γ-Aminobutyric acid (33.95, 102.25, 306.75 mg/kg; p.o.; single dose) can enhance the sleep of mice[6].
    γ-Aminobutyric acid (1, 2, 4 mg/kg/d; p.o.; 30 d) alleviates anxiety and restored food utilization rate in rats, with impairment induced by Di(2-ethylhexyl) phthalate (DEHP) exposure[7].

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    Animal Model: Pathogens free (SPF) Bagg’s albino (Balb/c) mice (18–20 g, 8 weeks old)[6]
    Dosage: 33.95, 102.25, 306.75 mg/kg
    Administration: Oral gavage; single dose; 20 mL/kg administration; measured in an hour
    Result: Prolonged the sleep duration, increased sleep rate, and shorten the sleep latency more effectively.
    Animal Model: Sprague-Dawley rat indued by DEHP (HY-B1945) (500 mg/kg)[7]
    Dosage: 1, 2, 4 mg/kg
    Administration: Oral gavage; combined administration; for 30 consecutive days
    Result: Reduced the levels of nitric oxide and nitric oxide synthase in rats treated with DEHP.
    Molecular Weight

    103.12

    Formula

    C4H9NO2

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    O=C(O)CCCN

    Structure Classification
    Initial Source

    mammalian central nervous system

    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    RT, protect from light

    In solvent -80°C 1 year
    -20°C 6 months
    Solvent & Solubility
    In Vitro: 

    H2O : 50 mg/mL (484.87 mM; Need ultrasonic)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 9.6974 mL 48.4872 mL 96.9744 mL
    5 mM 1.9395 mL 9.6974 mL 19.3949 mL
    View the Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

    • Molarity Calculator

    • Dilution Calculator

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

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    In Vivo:

    For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
    The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

    • Protocol 1

      Add each solvent one by one:  PBS

      Solubility: 100 mg/mL (969.74 mM); Clear solution; Need ultrasonic and warming and heat to 60°C

    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

    Dosage

    mg/kg

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    (per animal)

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    (per animal)

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    Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
    Calculation results:
    Working solution concentration: mg/mL
    This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.
    The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact MedChemExpress (MCE).
    Purity & Documentation

    Purity: 99.71%

    References

    Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    H2O 1 mM 9.6974 mL 48.4872 mL 96.9744 mL 242.4360 mL
    5 mM 1.9395 mL 9.6974 mL 19.3949 mL 48.4872 mL
    10 mM 0.9697 mL 4.8487 mL 9.6974 mL 24.2436 mL
    15 mM 0.6465 mL 3.2325 mL 6.4650 mL 16.1624 mL
    20 mM 0.4849 mL 2.4244 mL 4.8487 mL 12.1218 mL
    25 mM 0.3879 mL 1.9395 mL 3.8790 mL 9.6974 mL
    30 mM 0.3232 mL 1.6162 mL 3.2325 mL 8.0812 mL
    40 mM 0.2424 mL 1.2122 mL 2.4244 mL 6.0609 mL
    50 mM 0.1939 mL 0.9697 mL 1.9395 mL 4.8487 mL
    60 mM 0.1616 mL 0.8081 mL 1.6162 mL 4.0406 mL
    80 mM 0.1212 mL 0.6061 mL 1.2122 mL 3.0304 mL
    100 mM 0.0970 mL 0.4849 mL 0.9697 mL 2.4244 mL

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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