CAS 3063-05-6

L-Leucyl-L-phenylalanine

Description:

L-Leucyl-L-phenylalanine, with the CAS number 3063-05-6, is a dipeptide composed of the amino acids leucine and phenylalanine linked by a peptide bond. This compound is characterized by its hydrophobic nature due to the presence of both leucine and phenylalanine, which are non-polar amino acids. It typically exhibits a high melting point and is soluble in polar solvents, such as water, due to the presence of the amino and carboxyl functional groups. L-Leucyl-L-phenylalanine is often studied for its potential biological activities, including its role in protein synthesis and its influence on metabolic pathways. Additionally, it may have applications in the food and pharmaceutical industries, particularly in formulations aimed at enhancing flavor or nutritional value. The stability of this dipeptide can be affected by factors such as pH and temperature, which are important considerations in both laboratory and industrial settings. Overall, L-Leucyl-L-phenylalanine serves as an important model compound for understanding peptide behavior and interactions in biological systems.

Formula: C₁₅H₂₂N₂O₃

InChI: 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)/t12-,13-/m0/s1

InChI key: InChIKey=KFKWRHQBZQICHA-STQMWFEESA-N

SMILES: C([C@H](NC([C@H](CC(C)C)N)=O)C(O)=O)C1=CC=CC=C1

Synonyms:

• 165: PN: WO2010045512 SEQID: 174 unclaimed protein
• 218: PN: EP2161028 PAGE: 11 claimed protein
• 301: PN: WO2014145242 PAGE: 31 claimed protein
• 326: PN: WO2010059829 SEQID: 354 unclaimed protein
• 45: PN: WO2020097235 SEQID: 274 claimed protein
• <span class="text-smallcaps">L</smallcap>-Leucyl-<smallcap>L</span>-phenylalanine
• <span class="text-smallcaps">L</smallcap>-Phenylalanine, <smallcap>L</span>-leucyl-
• <span class="text-smallcaps">L</smallcap>-Phenylalanine, N-<smallcap>L</span>-leucyl-
• Alanine, N-<span class="text-smallcaps">L</smallcap>-leucyl-3-phenyl-, <smallcap>L</span>-
• Alanine, N-<span class="text-smallcaps">L</span>-leucyl-3-phenyl-
• Alanine, N-leucyl-3-phenyl-
• L-Leucyl-L-phenylalanine
• Leucylphenylalanine
• NSC 89191
• L-Phenylalanine, L-leucyl-
• L-Phenylalanine, N-L-leucyl-
• Alanine, N-L-leucyl-3-phenyl-

H-Leu-Phe-OH

CAS: 3063-05-6

A competitive inhibitor of both the peptidase and the esterase activities of carboxypeptidase Y. LF forms nanotubes.

Formula: C₁₅H₂₂N₂O₃

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 278.35

Ref: 01-4000185

H-Leu-Phe-OH

CAS: 3063-05-6

Formula: C₁₅H₂₂N₂O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 278.3468

Ref: IN-DA0030PV

Leucyl-phenylalanine

CAS: 3063-05-6

Leucyl-phenylalanine

Purity: ≥98%

Molecular weight: 278.35g/mol

Ref: 54-BUP16424

Leucyl-phenylalanine

CAS: 3063-05-6

Leucyl-phenylalanine (H-LEU-PHE-OH) is a dipeptide compound that can be used for protein synthesis.

Formula: C₁₅H₂₂N₂O₃

Purity: 99.47%

Color and Shape: Solid

Molecular weight: 278.35

Ref: TM-T19404

H-Leu-Phe-OH

CAS: 3063-05-6

H-Leu-Phe-OH is a synthetic substrate that has been shown to bind to neutrophils and induce chemotactic activity. H-Leu-Phe-OH binds to the receptor on the surface of neutrophils and increases their recruitment to sites of inflammation. Studies have shown that H-Leu-Phe-OH can also stimulate production of interleukin, which may be useful in treating systemic diseases such as chronic kidney disease. H-Leu-Phe-OH is expressed at high levels in glomeruli, where it is secreted into the glomerular filtrate by proximal tubules. The biological effects of this substance are mediated by intracellular calcium ion release from intracellular stores, which leads to increased levels of messenger RNA for monoclonal antibody production and protein synthesis in neutrophils.

Formula: C₁₅H₂₂N₂O₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 278.35 g/mol

Ref: 3D-FL108098

Leucyl-phenylalanine

CAS: 3063-05-6

Purity: 98%

Molecular weight: 278.3519897

Ref: 10-F603088