aminobutanoic acid formula

  • gamma-Aminobutyric acid - Wikipedia

    GABA transaminase enzyme catalyzes the conversion of 4-aminobutanoic acid (GABA) and 2-oxoglutarate (α-ketoglutarate) into succinic semialdehyde and glutamate. Succinic semialdehyde is then oxidized into succinic acid by succinic semialdehyde dehydrogenase and as such enters the citric acid cycle as a usable source of energy.

  • gamma-aminobutyric acid, 56-12-2

    the most common inhibitory neurotransmitter in the central nervous system. gamma-Aminobutyric acid is the chief inhibitory neurotransmitter in the mammalian central nervous system. It plays a role in regulating neuronal excitability throughout the nervous system. In humans, GABA is also directly responsible for the regulation of muscle tone.

  • carboxylic acid | Structure, Properties, Formula, Uses ...

    Its IUPAC name is 4-aminobutanoic acid. GABA is an inhibitory neurotransmitter in the central nervous system of humans. Salts of carboxylic acids are named in the same manner as are the salts of inorganic compounds ; the cation is named first and then the anion, as in sodium chloride .

  • 4-Aminobutanoic acid - webbook.nist.gov

    , The enthalpies of combustion and formation of some isomers of aminobutyric (aminobutanoic) acid, Rev. Roum. Chim., 1994, 39, 1391-1395. [ all data ] Skoulika and Sabbah, 1983

  • gamma-Aminobutyric acid - SpectraBase

    Compound gamma-Aminobutyric acid with free spectra: 8 NMR, 2 FTIR, and 1 Raman.

  • 3-Aminobutanoic acid - PubChem

    Description3-aminobutyrate is classified as a beta amino acid or a Beta amino acid derivative. Beta amino acids are amino acids having a (-NH2) group attached to the beta carbon atom. 3-aminobutyrate is considered to be a soluble (in water) and a weak acidic compound. 3-aminobutyrate can be found in feces.

  • 2-Aminobutanoic acid | C4H9NO2 | ChemSpider

    An <locant>alpha</locant>-amino acid that is butyric acid bearing a single amino substituent located at position 2. ChEBI CHEBI:35621 An alpha-amino acid that is butyric acid bearing a single amino substituent located at position 2.

  • 4-Aminobutyric Acid +99%, ACROS Organics | Fisher Scientific

    Linear Formula: H 2 N(CH 2) 3 CO 2 H: Beilstein: 04,413: Merck Index: 15,425: Solubility Information: Solubility in water: very soluble. Other solubilities: slightly soluble in common solvents: Formula Weight: 103.12: Physical Form: Crystalline Powder: Percent Purity ≥99.0% (on anhydrous substance) Chemical Name or Material: 4-Aminobutyric acid, 99+% Show More Show Less

  • Substance Name: Gamma-aminobutyric acid [JAN]

    56-12-2 - BTCSSZJGUNDROE-UHFFFAOYSA-N - Gamma-aminobutyric acid [JAN] - Similar structures search, synonyms, formulas, resource links, and other chemical information.

  • 4-aminobutyric acid Structure - C4H9NO2 - Over 100 million ...

    The 2D chemical structure image of 4-aminobutyric acid is also called skeletal formula, which is the standard notation for organic molecules. The carbon atoms in the chemical structure of 4-aminobutyric acid are implied to be located at the corner(s) and hydrogen atoms attached to carbon atoms are not indicated – each carbon atom is considered to be associated with enough hydrogen atoms to ...

  • L-a-Aminobutyric acid - Chem-Impex International

    L-α-Aminobutyric acid. Chem-Impex International; Catalog; Unusual Amino Acids and Derivatives ; Building Blocks for Peptide Synthesis

  • 4-Aminobutyric acid | 56-12-2

    Visit ChemicalBook To find more 4-Aminobutyric acid(56-12-2) information like chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight, physical properties,toxicity information,customs codes.

  • Fmoc-L-a-aminobutyric acid - Chem-Impex International

    Chem-Impex International; Catalog; Unusual Amino Acids and Derivatives ; Building Blocks for Peptide Synthesis ; Aminobutyric acid [Abu] a-Aminobutyric acid

  • 4-Aminobutanoic acid - CAS-Number 56-12-2 - chemodex.com

    GABA (CDX-G0043), CAS 56-12-2 is a high purity and quality chemical. Used as Amino acid, inhibitory neurotransmitter and immunomodulator. Amino acid, inhibitory neurotransmitter, immunomodulator

  • gamma-Aminobutyric acid - Wikipedia

    γ-Aminobutyric acid ( /ˈɡæmə əˈmiːnoʊbjuːˈtɪrᵻk ˈæsᵻd/; or GABA /ˈɡæbə/) is the chief inhibitory neurotransmitter in the mammalian central nervous seestem. It plays the principal role in reducin neuronal excitability throuoot the nervous seestem. In humans, GABA is an aa directly responsible for the regulation o muscle tone.

  • mzCloud – 2 Aminobutyric acid

    87 mass spectra in 1 spectral trees are available online for the compound 2-Aminobutyric acid . Last modification occurred on 11/5/2014 8:13:25 AM. mzCloud ‒ Free Online Mass Spectrometry Database

  • DL-2-Aminobutyric acid - 1H NMR Spectrum - SpectraBase

    1H Nuclear Magnetic Resonance (NMR) Spectrum of DL-2-Aminobutyric acid with properties.

  • 3-Aminobutanoic acid | C4H9NO2 - PubChem

    3-Aminobutanoic acid | C4H9NO2 | CID 10932 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities ...

  • L(+)-2-Aminobutyric acid, 98%, ACROS Organics | Fisher Scientific

    L(+)-2-Aminobutyric acid, 98%, ACROS Organics 1g; Glass bottle Chemicals:Organic Compounds:Organic acids and derivatives:Carboxylic acids and derivatives:Amino acids, peptides,

  • aminobutyric acid | Sigma-Aldrich

    Summary: Gamma-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor.

  • 2-Aminobutanoic acid | CAS#:2835-81-6 | Chemsrc

    Chemsrc provides 2-Aminobutanoic acid(CAS#:2835-81-6) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of 2-Aminobutanoic acid are included as well.

  • γ-Aminobutyric acid | C4H9NO2 | ChemSpider

    Structure, properties, spectra, suppliers and links for: γ-Aminobutyric acid, gamma-Aminobutyric acid, 56-12-2.

  • Aminobutyric Acid (Abu), Unusual Amino Acids, Amino Acids, P3 ...

    Review Aminobutyric Acid (Abu) and other Unusual Amino Acids products from P3 BioSystems, a US supplier of high quality peptides and peptide synthesis products JavaScript seems to be disabled in your browser.

  • 4-aminobutyric acid - Registration Dossier - ECHA

    4-aminobutyric acid EC Number: 200-258-6 EC Name: 4-aminobutyric acid CAS Number: 56-12-2 Molecular formula: C4H9NO2 IUPAC Name: 4-aminobutanoic acid . Type of substance

  • 3-aminobutyric acid | Sigma-Aldrich

    Summary: The neurotransmitter gamma-aminobutyric acid (GABA) functions in the central nervous system to regulate synaptic transmission of neurons. This gene encodes one of three related subunits, which combine as homo- or hetero-pentamers to form GABA(C) receptors.

  • 4-Aminobutanoic acid - NIST

    4-Aminobutanoic acid. Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript . Other names: γ-Aminobutyric acid; 4-Aminobutyric acid; 4-Amino-n-butyric acid; γ-Amino-n-butyric acid; Butanoic acid, 4-amino-; γ-Aminobutanoic...

  • 4-Aminobutyric acid - InvivoChem

    Description: Gamma-Aminobutyric Acid (4-Aminobutanoic acid, GABA, Gamma-aminobutyric acid, Piperidic acid) is a naturally occurring neurotransmitter with central nervous system (CNS) inhibitory activity. γ-Aminobutyric acid (GABA) functions primarily as an inhibitory neurotransmitter in the mature central nervous system. The addition of GABA into the cell culture medium promoted the proliferation of GABRP-expressing PDAC cells, but not GABRP-negative cells, and GABAA receptor antagonists ...

  • alpha-Aminobutyric acid - Wikipedia

    Infobox references α-Aminobutyric acid (AABA), also known as homoalanine in biochemistry, is a non-proteinogenic alpha amino acid with chemical formula C 4 H 9 NO 2. The straight two carbon side chain is one carbon longer than alanine, hence the prefix homo-.