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100g Pack Size. Group: Analytical Reagents, Biochemicals, Building Blocks, Flavours and Fragrance Materials. Formula: C4H9NO2. CAS No. 56-12-2. Prepack ID 32215466-100g. Molecular Weight 103.12. See USA prepack pricing.
4-Aminobutyric acid-15N
98 atom % 15N. Group: Fluorescence/luminescence spectroscopy.
4-Aminobutyric acid-2,2,3,3,4,4-d6
4-Aminobutyric acid-2,2,3,3,4,4-d6. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-AMINOBUTYRIC ACID-2,2,3,3,4,4-D6;4-AMINOBUTYRIC-2,2,3,3,4,4-D6 ACID;GABA-D6. Product Category: Heterocyclic Organic Compound. CAS No. 70607-85-1. Molecular formula: H2N(CD2)3CO2H. Mole weight: 109.16. Purity: 99 atom % D. Product ID: ACM70607851. Alfa Chemistry ISO 9001:2015 Certified.
4-Aminobutyric acid-2,2,3,3,4,4-d6
97 atom % D. Group: Fluorescence/luminescence spectroscopy.
4-Aminobutyric acid-2,2-d2
4-Aminobutyric acid-2,2-d2. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-Aminobutyric acid-2,2-d2;4-Aminobutyric-2,2-D2 acid (Gaba). Product Category: Heterocyclic Organic Compound. CAS No. 67910-98-9. Molecular formula: H2N(CH2)2CD2CO2H. Mole weight: 105.13. Purity: 98 atom % D. Product ID: ACM67910989. Alfa Chemistry ISO 9001:2015 Certified.
4-Aminobutyric acid-2,2-d2
98 atom % D. Group: Fluorescence/luminescence spectroscopy.
A cleavable biotin crosslinker. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences.
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N-Methyl-4-aminobutyric Acid
A GABA derivative and hydrolysis product of the industrial solvent, N-methyl-2-pyrrolidinone. Biologically it is a product of nicotine catabolism in bacteria and inhibits L-Carnitine from undergoing β-oxidation in mammals. It is commonly found in skin products to prevent wrinkles. Group: Biochemicals. Alternative Names: 4-(Methylamino)butanoic Acid; N-Methyl-GABA; N-Methyl-γ-aminobutyric Acid; 4-(Methylamino)butyric Acid. Grades: Highly Purified. CAS No. 1119-48-8. Pack Sizes: 250mg. US Biological Life Sciences.
Worldwide
N-Methyl-4-aminobutyric Acid-d3
A labeled GABA derivative and hydrolysis product of the industrial solvent, N-methyl-2-pyrrolidinone. Biologically it is a product of nicotine catabolism in bacteria and inhibits L-Carnitine from undergoing β-oxidation in mammals. It is commonly found in skin products to prevent wrinkles. Group: Biochemicals. Alternative Names: 4-(Methylamino)butanoic Acid-d3; N-Methyl-GABA-d3; N-Methyl-γ-aminobutyric Acid-d3; 4-(Methylamino)butyric Acid-d3. Grades: Highly Purified. CAS No. 1215511-11-7. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
N-Nitroso-n-methyl-4-aminobutyric acid
N-Nitroso-n-methyl-4-aminobutyric acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-(Methylnitrosoamino)butanoic acid. Product Category: Promotional Products. Appearance: yellow oil. CAS No. 61445-55-4. Molecular formula: C5H10N2O3. Mole weight: 146.14. Purity: 95+%. IUPACName: 4-[methyl(nitroso)amino]butanoic acid. Product ID: ACM61445554-1. Alfa Chemistry ISO 9001:2015 Certified.
N-Nitroso-N-methyl-4-aminobutyric Acid-d3
This N-nitrosamino acid has been isolated and identified in various types of tobacco, inlcluding snuff, chewing and pipe tobacco, cigars and cigarettes. The occurence of N-nitrosamino acids are highly correlated with levels of tobacco-specific N-nitrosamines which are known carcinogens in a wide range of animal species. Group: Biochemicals. Alternative Names: 4-[ (Methyl-d3) nitrosoamino) ]butanoic Acid; N- (Methyl-d3) -N- (3-carboxypropyl) nitrosamine. Grades: Highly Purified. CAS No. 1184996-41-5. Pack Sizes: 5mg. US Biological Life Sciences.
The methyl ester of the nitrosamino acid, N-Nitroso-N-methylaminobutyric acid. This N-nitrosamino acid has been isolated and identified in various types of tobacco, including snuff, chewing and pipe tobacco, cigars and cigarettes. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg. US Biological Life Sciences.
Worldwide
N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)
This N-nitrosamino acid has been isolated and identified in various types of tobacco, inlcluding snuff, chewing and pipe tobacco, cigars and cigarettes. The occurence of N-nitrosamino acids are highly correlated with levels of tobacco-specific N-nitrosamines which are known carcinogens in a wide range of animal species. Group: Biochemicals. Alternative Names: 4- (Methylnitrosoamino) butanoic Acid; N-Methyl-N- (3-carboxypropyl) nitrosamine; NMB. Grades: Highly Purified. CAS No. 61445-55-4. Pack Sizes: 100mg. Molecular Formula: C?H??N?O?, Molecular Weight: 146.15. US Biological Life Sciences.
(2E, 4S) -5-[1, 1'-Biphenyl]-4-yl-4-[[ (1, 1-dimethylethoxy) carbonyl]amino]-2-methyl-2-pentenoic Acid was used in the study to process for preparation of biaryl-substituted 4-aminobutyric acids by hydrogenation of the corresponding alkenoates. Group: Biochemicals. Grades: Highly Purified. CAS No. 1015037-46-3. Pack Sizes: 10mg, 25mg. Molecular Formula: C23H27NO4, Molecular Weight: 381.46. US Biological Life Sciences.
Worldwide
4-aminobutyrate-pyruvate transaminase
Requires pyridoxal 5'-phosphate. The enzyme is found in plants that do not have the 2-oxoglutarate dependent enzyme (cf. EC 2.6.1.19). The reaction with pyruvate is reversible while the reaction with glyoxylate only takes place in the forward direction. Group: Enzymes. Synonyms: aminobutyrate aminotransferase (ambiguous); γ-aminobutyrate aminotransaminase (ambiguous); γ-aminobutyrate transaminase (ambiguous); γ-aminobutyric acid aminotransferase (ambiguous); γ-aminobutyric acid pyruvate transamin. Enzyme Commission Number: EC 2.6.1.96. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2937; 4-aminobutyrate-pyruvate transaminase; EC 2.6.1.96; aminobutyrate aminotransferase (ambiguous); γ-aminobutyrate aminotransaminase (ambiguous); γ-aminobutyrate transaminase (ambiguous); γ-aminobutyric acid aminotransferase (ambiguous); γ-aminobutyric acid pyruvate transaminase; γ-aminobutyric acid transaminase (ambiguous); γ-aminobutyric transaminase (ambiguous); 4-aminobutyrate aminotransferase (ambiguous); 4-aminobutyric acid aminotransferase (ambiguous); aminobutyrate transaminase (ambiguous); GABA aminotransferase (ambiguous); GABA transaminase (ambiguous); GABA transferase; POP2 (gene name). Cat No: EXWM-2937.
An important inhibitory neurotransmitter. Foods that contain γ-aminobutyric acid (GABA) can have an immediate effect of suppressing autonomic nerve activity related to blood pressure increase. Reacts with isothiocyanates to produce thioureas which have antifungal activity. Acts as a GABAA and GABAB receptor agonist. Group: Biochemicals. Alternative Names: 4-Aminobutanoic Αcid; 3-Carboxypropylamine; 4-Aminobutyric Acid; Aminalon; GABA; Gaballon; Gamarex; Gammalon; Gammalone; Gammar; Gammasol; Mielogen; Mielomade; NSC 27418; NSC 32044; NSC 45460; NSC 51295; Oryza GABA Extract HC 90; Pharma-GABA 20S; Pharmagaba; Pharmagaba 20; Pharmagaba 20D; Piperidic acid; Piperidinic acid; γ-Aminobutanoic acid; γ-Aminobutyric Acid. Grades: Reagent Grade. CAS No. 56-12-2. Pack Sizes: 100g, 500g, 1Kg. US Biological Life Sciences.
γ-Aminobutyric acid (4-Aminobutyric acid) is a major inhibitory neurotransmitter in the adult mammalian brain, binding to the ionotropic GABA receptors ( GABA A receptors ) and metabotropic receptors ( GABA B receptors. γ-Aminobutyric acid shows calming effect by blocking specific signals of central nervous system [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: 4-Aminobutyric acid. CAS No. 56-12-2. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N0067.
Pivagabine (CXB 722) is a hydrophobic 4-aminobutyric acid derivative with neuromodulatory activity. Pivagabine penetrates the blood-brain barrier in rats. Pivagabine antagonizes the effects of foot shock on both GABAA receptor function and corticotropin-releasing factor (CRF) concentrations in rat brain [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CXB-722. CAS No. 69542-93-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-108295.
(R)-4-Amino-3-hydroxybutyric acid
(R)-4-Amino-3-hydroxybutyric acid ((R)-GABOB) is a 4-aminobutyric acids ( GABAB ) agonist. (R)-4-Amino-3-hydroxybutyric acid is promising for research of nervous disorders [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (-)-γ-Amino-β-hydroxybutyric acid; (R)-GABOB; (-)-β-Hydroxy-GABA. CAS No. 7013-7-2. Pack Sizes: 100 mg; 250 mg; 500 mg; 1 g; 5 g. Product ID: HY-W005749.
Requires pyridoxal phosphate. Some preparations also act on β-alanine, 5-aminopentanoate and (R,S)-3-amino-2-methylpropanoate. Group: Enzymes. Synonyms: β-alanine-oxoglutarate transaminase; aminobutyrate aminotransferase (ambiguous); β-alanine aminotransferase; β-alanine-oxoglutarate aminotransferase; γ-aminobutyrate aminotransaminase (ambiguous); γ-aminobutyrate transaminase (ambiguous); γ-aminobutyrate-α-ketoglutarate aminotransferase; γ-aminobutyrate-α-ketoglutarate transaminase; γ-aminobutyrate:α-oxoglutarate aminotransferase; γ-aminobutyric acid aminotransferase (ambiguous); γ-aminobutyric acid transaminase (ambiguous); γ-aminobutyric acid-α-ketoglutarate transaminase; γ-aminobutyric acid-α-ketoglutaric acid aminotransferase; γ-aminobutyric acid-2-oxoglutarate transaminase; γ-aminobutyric transaminase (ambiguous); 4-aminobutyrate aminotransferase (ambiguous); 4-aminobutyrate-2-ketoglutarate aminotransferase; 4-aminobutyrate-2-oxoglutarate aminotransferase;. Enzyme Commission Number: EC 2.6.1.19. CAS No. 9037-67-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2859; 4-aminobutyrate-2-oxoglutarate transaminase; EC 2.6.1.19; 9037-67-
Aminooxyacetic Acid
Aminooxyacetic acid, often abbreviated AOA or AOAA, is a GABA transaminase (GABA-T) inhibitor (Ki = 9.16 μM) that inhibits 4-aminobutyrate aminotransferase (GABA-T) activity in vitro and in vivo, leading to less gamma-aminobutyric acid (GABA) being broken down. Subsequently, the level of GABA is increased in tissues. At concentrations high enough to fully inhibit 4-aminobutyrate aminotransferase activity, aminooxyacetic acid is indicated as a useful tool to study regional GABA turnover in rats. AOAA is also an inhibitor of pyridoxal phosphate (PLP)-dependent enzymes, which serve as an inhibitor by attacking the Schiff base linkage between PLP and the enzyme, forming oxime type complexes. Uses: Gaba agents. Synonyms: Aminooxyacetate; AOAA; 2-Aminooxyacetic acid; U 7524; U7524; U-7524. Grades: ≥95%. CAS No. 645-88-5. Molecular formula: C2H5NO3. Mole weight: 91.07.
Vigabatrin
Vigabatrin is an analogue of gamma-aminobutyric acid(GABA) and is an irreversible inhibitor of 4-aminobutyrate transaminase. It is used in combination with other agents as therapy of refractory complex partial seizures and as monotherapy for infantile spasms. It is an antiepileptic drug that inhibits the breakdown of GABA by acting as a suicide inhibitor of GABA transaminase (GABA-T). It increases brain concentrations of GABA, an inhibitory neurotransmitter in the CNS, by irreversibly inhibiting enzymes that catabolize GABA or block the reuptake of GABA into glia and nerve endings. It may also work by suppressing repetitive neuronal firing through inhibition of voltage-sensitive sodium channels. It is a racemic compound, and its [S]-enantiomer is pharmacologically active. It has been listed. Uses: Vigabatrin is used in combination with other agents as therapy of refractory complex partial seizures and as monotherapy for infantile spasms. it is an antiepileptic drug. Synonyms: γ-Vinyl-GABA; 4-Amino-5-hexenoic Acid; (±)-4-Amino-5-hexenoic Acid; Sabril; Vigabatrine; 4-Aminohexenoic acid; rac-Vigabatrin; (±)-Vigabatrin; (±)-4-Aminohexenoic acid. Grades: ≥98%. CAS No. 68506-86-5. Molecular formula: C6H11NO2. Mole weight: 129.16.
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