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Merck

A3128

Sigma-Aldrich

L-Alanyl-L-phenylalanin

≥98% (TLC)

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About This Item

Empirische Formel (Hill-System):
C12H16N2O3
CAS-Nummer:
Molekulargewicht:
236.27
MDL-Nummer:
UNSPSC-Code:
12352202
PubChem Substanz-ID:
NACRES:
NA.26

product name

L-Alanyl-L-phenylalanin,

Assay

≥98% (TLC)

Qualitätsniveau

Form

powder

Farbe

white to off-white

Lagertemp.

−20°C

SMILES String

C[C@H](N)C(=O)N[C@@H](Cc1ccccc1)C(O)=O

InChI

1S/C12H16N2O3/c1-8(13)11(15)14-10(12(16)17)7-9-5-3-2-4-6-9/h2-6,8,10H,7,13H2,1H3,(H,14,15)(H,16,17)/t8-,10-/m0/s1

InChIKey

OMNVYXHOSHNURL-WPRPVWTQSA-N

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Amino Acid Sequence

Ala-Phe

Biochem./physiol. Wirkung

Alanyl dipeptides such as ala-leu, ala-lys, ala-gly, ala-pro, ala-tyr and ala-phe may be used in physicochemical studies or to evaluate dipeptide separation technologies. Alanyl dipeptides may also be used for studying cell uptake mechanisms, dipeptide metabolism or cell growth supplementation benefits.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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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
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
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
Yasuhito Shomura et al.
Protein science : a publication of the Protein Society, 21(5), 707-716 (2012-03-13)
BacD is an ATP-dependent dipeptide ligase responsible for the biosynthesis of L-alanyl-L-anticapsin, a precursor of an antibiotic produced by Bacillus spp. In contrast to the well-studied and phylogenetically related D-alanine: D-alanine ligase (Ddl), BacD synthesizes dipeptides using L-amino acids as

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