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N-Acetyl-L-glutamic acid, a glutamic acid, is a component of animal cell culturing media. N-Acetyl-L-glutamic acid is a metabolite of Saccharomyces cerevisiae and human [1]. Uses: Scientific research. Group: Natural products. CAS No. 1188-37-0. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g. Product ID: HY-W015240.
N-Acetyl-L-glutamic acid. Group: Biochemicals. Alternative Names: Ac-Glu-OH. Grades: Highly Purified. CAS No. 1188-37-0. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C7H11NO5. US Biological Life Sciences.
Worldwide
N-Acetyl-L-Glutamic acid
N-Acety-L-Glutamic acid is a biologically active compound that is found in the cells. It is a product of the urea cycle and has been shown to inhibit the activity of enzymes such as ester hydrochloride synthetase, which catalyzes the conversion of arginine and citrulline to ornithine and carbamoyl phosphate. N-Acetylglutamic acid also plays an important role in cellular physiology, such as transcriptional regulation and protein synthesis. Deficiency can lead to glutamate accumulation and neurological disorders such as epilepsy. The biochemical properties of N-acetylglutamic acid are still not well known, but it has been shown to react with ammonia to form glutamine. CAS No. 1188-37-0. Product ID: PAP-0020. Molecular formula: C7H11NO5. Category: Amino acid. Product Keywords: Amino Acid Series; N-Acetyl-L-Glutamic acid; PAP-0020; Amino acid; C7H11NO5; 1188-37-0. Color: White. EC Number: 214-708-4. Physical State: Solid. Solubility: 36g/l (Lit.). Storage: 2-8°C. Applications: N-Acetyl-L-Glutamic acid is a product of the urea cycle and has been shown to inhibit the activity of enzymes such as ester hydrochloride synthetase, which catalyzes the conversion of arginine and citrulline to ornithine and carbamoyl phosphate. N-Acetylglutamic acid also plays an important role in cellular physiology, such as transcriptional regulation and protein synthesis. Deficiency can lead to glutamate accumulation and neurological
N-Acetyl-L-glutamic Acid (non-animal)
≥ 98.0%. Group: Biochemicals. Grades: Molecular Biology Grade. Pack Sizes: 1Kg. US Biological Life Sciences.
Worldwide
Acetyl-L-glutamic acid
A substrate for acetylglutamate kinase. An inhibitor of N-acetyl-L-glutamate synthetase. Synonyms: Ac-L-Glu-OH. Grades: 98-102% (Assay). CAS No. 1188-37-0. Molecular formula: C7H11NO5. Mole weight: 189.17.
Acetyl tetrapeptide-9 acetate
Acetyl tetrapeptide-9 acetate can promote skin remodeling and help achieve firm and plump skin effects. It plays a role in the stimulation of basement membrane polysaccharide (lumican) and the synthesis of collagen I. Synonyms: Ac-Gln-Asp-Val-His-OH.CH3CO2H; Ac-QDVH.CH3CO2H; N-acetyl-L-glutaminyl-L-alpha-aspartyl-L-valyl-L-histidine acetic acid. Grades: ≥95%. CAS No. 2763583-72-6. Molecular formula: C24H37N7O11. Mole weight: 599.59.
amino-acid N-acetyltransferase
Also acts with L-aspartate and, more slowly, with some other amino acids. Group: Enzymes. Synonyms: N-acetylglutamate synthase; AGAS; acetylglutamate acetylglutamate synthetase; acetylglutamic synthetase; amino acid acetyltransferase; N-acetyl-L-glutamate synthetase; N-acetylglutamate synthetase. Enzyme Commission Number: EC 2.3.1.1. CAS No. 9029-88-3. 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-2037; amino-acid N-acetyltransferase; EC 2.3.1.1; 9029-88-3; N-acetylglutamate synthase; AGAS; acetylglutamate acetylglutamate synthetase; acetylglutamic synthetase; amino acid acetyltransferase; N-acetyl-L-glutamate synthetase; N-acetylglutamate synthetase. Cat No: EXWM-2037.
Dilithium N-acetyl-L-glutamate
Dilithium N-acetyl-L-glutamate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 32093-27-9, Dilithium N-acetyl-L-glutamate, CTK4G8201, EINECS 250-919-8, AG-F-07137, L-Glutamic acid,N-acetyl-, dilithium salt (9CI), Glutamicacid, N-acetyl-, dilithium salt, L- (8CI); Dilithium N-acetylglutamate. Product Category: Heterocyclic Organic Compound. CAS No. 32093-27-9. Molecular formula: C7H9Li2NO5. Mole weight: 201.032060 [g/mol]. Purity: 0.96. IUPACName: dilithium;(2S)-2-acetamidopentanedioate. Canonical SMILES: [Li+].[Li+].CC(=O)NC(CCC(=O)[O-])C(=O)[O-]. ECNumber: 250-919-8. Product ID: ACM32093279. Alfa Chemistry ISO 9001:2015 Certified.
N-Acetyl-L-Glutamine
N-acetyl-L-glutamine is an N(2)-acetylglutamine that has L-configuration. It has a role as a human metabolite. It is a N-acetyl-L-amino acid, a N(2)-acyl-L-glutamine and a N(2)-acetylglutamine. It is a conjugate acid of a N-acetyl-L-glutaminate. It is an enantiomer of a N(2)-acetyl-D-glutamine. CAS No. 2490-97-3. Product ID: PAP-0011. Molecular formula: C7H12N2O4. Category: Amino acid. Product Keywords: Amino Acid Series; N-Acetyl-L-Glutamine; PAP-0011; Amino acid; C7H12N2O4; 2490-97-3. Color: White to Off-White. EC Number: 219-647-7. Physical State: Solid. Solubility: DMSO (Slightly, Heated, Sonicated), Water (Sparingly, Heated, Sonicated). Storage: Sealed in dry,Room Temperature. Applications: N-Acety-L-Glutamine is an amino acid that is not synthesized by the human body and must be obtained through diet. It is a precursor to glutamate, which is an important neurotransmitter in the brain. N-Acetyl-L-glutamine has been shown to have neuroprotective effects against various metabolic disorders including diabetes, bowel disease, and microdialysis probes. The effect of N-acetyl-L-glutamine on neuronal death can be observed using a reaction solution containing sodium citrate and glucose injection. N-acetylglutamine has been shown to increase the activity of enzymes such as citrate synthase in this reaction solution. Boiling Point: 430.5±40.0 °C(Predicted). Melting Point: 206-208 °C. Density: 1.290±0.06 g/cm3(Predi