CAS 7669-65-0

L-Phenylalanyl-L-proline

Description:

L-Phenylalanyl-L-proline, also known by its CAS number 7669-65-0, is a dipeptide composed of the amino acids phenylalanine and proline. This compound features a unique structure that combines the aromatic side chain of phenylalanine with the cyclic structure of proline, contributing to its distinct properties. It is typically characterized by its role in protein synthesis and its potential influence on biological processes due to its specific amino acid composition. L-Phenylalanyl-L-proline may exhibit various biological activities, including potential neuroprotective effects and involvement in signaling pathways. In terms of solubility, it is generally soluble in water, which is typical for many peptides, and it may also exhibit stability under physiological conditions. Its synthesis can be achieved through peptide coupling methods, making it of interest in pharmaceutical and biochemical research. Overall, L-Phenylalanyl-L-proline serves as a valuable compound in the study of peptides and their applications in health and disease.

Formula: C₁₄H₁₈N₂O₃

InChI: InChI=1S/C14H18N2O3/c15-11(9-10-5-2-1-3-6-10)13(17)16-8-4-7-12(16)14(18)19/h1-3,5-6,11-12H,4,7-9,15H2,(H,18,19)/t11-,12-/m0/s1

InChI key: InChIKey=WEQJQNWXCSUVMA-RYUDHWBXSA-N

SMILES: C([C@H](CC1=CC=CC=C1)N)(=O)N2[C@H](C(O)=O)CCC2

Synonyms:

• 26: PN: WO2021055880 SEQID: 27 claimed protein
• <span class="text-smallcaps">L</smallcap>-Phenylalanyl-<smallcap>L</span>-proline
• <span class="text-smallcaps">L</smallcap>-Proline, 1-<smallcap>L</span>-phenylalanyl-
• <span class="text-smallcaps">L</smallcap>-Proline, <smallcap>L</span>-phenylalanyl-
• H-Phe-Pro-OH
• Proline, 1-(3-phenyl-<span class="text-smallcaps">L</smallcap>-alanyl)-, <smallcap>L</span>-
• Proline, 1-(3-phenyl-<span class="text-smallcaps">L</span>-alanyl)-
• Proline, 1-(3-phenyl-L-alanyl)-
• L-Phenylalanyl-L-proline
• Proline, 1-(3-phenyl-L-alanyl)-, L-
• L-Proline, 1-L-phenylalanyl-

H-Phe-Pro-OH

CAS: 7669-65-0

Substrate for skin fibroblast prolidase.

Formula: C₁₄H₁₈N₂O₃

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 262.31

Ref: 01-4005005

H-Phe-pro-oh

CAS: 7669-65-0

Formula: C₁₄H₁₈N₂O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 262.3043

Ref: IN-DA005VLQ

(S)-1-((S)-2-Amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid

CAS: 7669-65-0

(S)-1-((S)-2-Amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid

Purity: 98%

Molecular weight: 262.31g/mol

Ref: 54-OR1068072

(S)-1-((S)-2-Amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid

CAS: 7669-65-0

(S)-1-((S)-2-Amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid, with catalog number T65393 and CAS number 7669-65-0, is an important organic compound used in life sciences research.

Formula: C₁₄H₁₈N₂O₃

Color and Shape: Solid

Molecular weight: 262.309

Ref: TM-T65393

H-Phe-Pro-OH

CAS: 7669-65-0

H-Phe-Pro-OH is a cyclic peptide that is a structural mimic of the natural amino acid gamma-aminobutyric acid (GABA) and has been shown to be an effective inhibitor of the p450 enzymes responsible for carcinogen activation. The peptide binds to response elements in DNA and RNA, which prevents transcription of genes that are involved in cancer development. H-Phe-Pro-OH also inhibits collagen production and has hemolytic activity due to hydrogen bonding with erythrocytes. This peptide can be used as an antimicrobial agent against Gram negative bacteria, including Pseudomonas aeruginosa, Klebsiella pneumoniae, Escherichia coli, and Salmonella typhimurium. In addition, it has been shown to inhibit the growth of Gram positive bacteria such as Staphylococcus aureus and Clostridium perfringens. The mechanism by which this compound inhibits bacterial growth is

Formula: C₁₄H₁₈N₂O₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 262.3 g/mol

Ref: 3D-FP108146