A1416
β-Ala-Phe
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About This Item
Empirical Formula (Hill Notation):
C12H16N2O3
CAS Number:
Molecular Weight:
236.27
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
InChI
1S/C12H16N2O3/c13-7-6-11(15)14-10(12(16)17)8-9-4-2-1-3-5-9/h1-5,10H,6-8,13H2,(H,14,15)(H,16,17)/t10-/m0/s1
SMILES string
NCCC(=O)N[C@@H](Cc1ccccc1)C(O)=O
InChI key
FLJLAJANCPPHDW-JTQLQIEISA-N
storage temp.
−20°C
Regulatory Information
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Zhi-Xia Zheng et al.
Electrophoresis, 26(4-5), 1007-1012 (2005-02-17)
A ligand-exchange capillary electrophoresis was explored, with L-ornithine as the ligand and copper(II) as the central ion. Its applicability was demonstrated with underivatized and dansyl amino acids, a dipeptide, and drugs with amino alcohol structure. The enantioselectivity was found to
J Li et al.
Electrophoresis, 20(1), 171-179 (1999-03-05)
The separation of stereoisomers, particularly enantiomers, is important when their physiological activity differs. We have resolved the four stereoisomers each of alanylphenylalanine (Ala-Phe) and of leucylphenylalanine (Leu-Phe) by capillary electrophoresis using beta-cyclodextrin as a buffer additive and urea to enhance
Xiao-Lin Zhu et al.
Journal of agricultural and food chemistry, 55(21), 8367-8371 (2007-10-12)
A replicate heart-cut column-switching HPLC method combined with two switching valves was newly developed for the simultaneous determination of three antihypertensive peptides (Ala-Phe, Tyr-Pro, and Trp-Tyr) in tryptic casein hydrolysate in one run-in assay. After a first separation on an
Kyung Min Choi et al.
Analytical biochemistry, 367(2), 167-172 (2007-06-30)
A spectrophotometric assay to determine peptide transport has been developed. Using two chromogenic peptide mimetics, L-phenylalanyl-L-2-sulfanilylglycine (PSG) and L-phenylalanyl-L-3-thiaphenylalanine (PSP), the peptide transport patterns in individual cell species can be evaluated effectively. After the addition of PSG to a HeLa
Tomasz Pawlak et al.
The journal of physical chemistry. B, 116(6), 1974-1983 (2012-01-14)
DFT methods were employed to compute the (13)C NMR chemical shift tensor (CST) parameters for crystals of YAF peptides (Tyr-Ala-Phe) with different stereochemistry for the Ala residue. Tyr-D-Ala-Phe 1 crystallizes in the C2 space group while Tyr-L-Ala-Phe crystallizes in either
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