Product Name :
3-Aminobutanoic acid (CAS 541-48-0)
Synonym :
(±)-3-Aminobutyric acid; DL-3-Aminobutyric acid
Application :
3-Aminobutanoic acid is a biochemical used in proteomics research
CAS:
541-48-0
Purity:
Molecular Weight:
103.12
Formula :
C4H9NO2
Physical state:
Solid
solubility :
Shipping Condition :
Store at room temperature
Melting point:
189° C (dec.)
SMILES:
CC(CC(=O)O)N
References:
:CuI-catalyzed coupling reaction of beta-amino acids or esters with aryl halides at temperature lower than that employed in the normal Ullmann reaction.20781-20-8 supplier Facile synthesis of SB-214857.148893-10-1 supplier | Ma, D.PMID:33427133 and Xia, C. 2001. Org Lett. 3: 2583-6. PMID: 11483066Direct high-performance liquid chromatographic enantioseparation of apolar beta-amino acids on a quinine-derived chiral anion-exchanger stationary phase. | Péter, A. 2002. J Chromatogr A. 955: 141-50. PMID: 12061560Direct and indirect high-performance liquid chromatographic enantioseparation of beta-amino acids. | Péter, A., et al. 2004. J Chromatogr A. 1031: 171-8. PMID: 15058580Liquid chromatographic resolution of beta-amino acids on CSPs based on optically active (3,3′-diphenyl-1,1′-binaphthyl)-20-crown-6. | Choi, HJ., et al. 2008. Anal Chim Acta. 619: 122-8. PMID: 18539184Studies on Cu(II) ternary complexes involving an aminopenicillin drug and imidazole containing ligands. | Regupathy, S. and Nair, MS. 2010. Spectrochim Acta A Mol Biomol Spectrosc. 75: 656-63. PMID: 20034849Synthesis of N-substituted acyclic beta -amino acids and their investigation as GABA uptake inhibitors. | Sitka, I., et al. 2013. Eur J Med Chem. 65: 487-99. PMID: 23770450Deaminative and decarboxylative catalytic alkylation of amino acids with ketones. | Kalutharage, N. and Yi, CS. 2013. Angew Chem Int Ed Engl. 52: 13651-5. PMID: 24174407Biochemical characterization and structural insight into aliphatic beta -amino acid adenylation enzymes IdnL1 and CmiS6. | Cieślak, J., et al. 2017. Proteins. 85: 1238-1247. PMID: 28316096Dataset on collecting volatile compounds produced by three bacteria and testing their efficacy against the pathogen Peronophythora litchii. | Zheng, L., et al. 2019. Data Brief. 25: 104345. PMID: 31485468New Sipanmycin Analogues Generated by Combinatorial Biosynthesis and Mutasynthesis Approaches Relying on the Substrate Flexibility of Key Enzymes in the Biosynthetic Pathway. | Malmierca, MG., et al. 2020. Appl Environ Microbiol. 86: PMID: 31732573Urinary metabolomics analysis reveals the anti-diabetic effect of stachyose in high-fat diet/streptozotocin-induced type 2 diabetic rats. | Liang, L., et al. 2020. Carbohydr Polym. 229: 115534. PMID: 31826396Structure-function investigation of 3-methylaspartate ammonia lyase reveals substrate molecular determinants for the deamination reaction. | Saez-Jimenez, V., et al. 2020. PLoS One. 15: e0233467. PMID: 32437404Combined supplementation of sodium humate and glutamine reduced diarrhea incidence of weaned calves by intestinal microbiota and metabolites changes. | Wang, D., et al. 2021. J Anim Sci. 99: PMID: 34673954Vascular Endothelial Growth Factor May Be Involved in the Behavioral Changes of Progeny Rats after Exposure to Ceftriaxone Sodium during Pregnancy. | Yang, X., et al. 2022. J Microbiol Biotechnol. 32: 699-708. PMID: 35484974