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Merck
CN

SMB00982

Sigma-Aldrich

L-Leucyl-L-phenylalanine

Synonym(s):

N-L-Leucyl-L-phenylalanine, N-Leucyl-3-phenylalanine, N-Leucylphenylalanine, L-Leu-L-Phe, Leu-phe, Leucine phenylalanine dipeptide, Leucyl-phenylalanine, Leucylphenylalanine

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About This Item

Empirical Formula (Hill Notation):
C15H22N2O3
CAS Number:
Molecular Weight:
278.35
MDL number:
UNSPSC Code:
12352209
NACRES:
NA.26
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Assay

≥95% (HPLC)

Quality Level

form

solid

mp

218—220 °C

storage temp.

2-8°C

SMILES string

[N+H3]C(CC(C)C)C(=O)NC(Cc1ccccc1)C(=O)[O-]

InChI

1S/C15H22N2O3/c1-10(2)8-12(16)14(18)17-13(15(19)20)9-11-6-4-3-5-7-11/h3-7,10,12-13H,8-9,16H2,1-2H3,(H,17,18)(H,19,20)

InChI key

KFKWRHQBZQICHA-UHFFFAOYSA-N

General description

L-Leucyl-L-phenylalanine, a dipeptide, is an incomplete breakdown product of protein digestion or protein catabolism.

Application

ʟ-Leucyl-ʟ-phenylalanine can be used in biochemical and metabolomics research applications

Features and Benefits

  • Suitable for Metabolomics and Biochemical research
  • High-quality compound suitable for multiple research applications

Other Notes

For additional information on our range of Biochemicals, please complete this form.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

动植物源性产品
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Dustin G Brown et al.
Cancer & metabolism, 4, 11-11 (2016-06-09)
Colorectal cancers (CRC) are associated with perturbations in cellular amino acids, nucleotides, pentose-phosphate pathway carbohydrates, and glycolytic, gluconeogenic, and tricarboxylic acid intermediates. A non-targeted global metabolome approach was utilized for exploring human CRC, adjacent mucosa, and stool. In this pilot

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