CAS 107573-17-1
:alanyl-phenylalanyl-lysine fluoromethane
Description:
Alanyl-phenylalanyl-lysine fluoromethane, identified by the CAS number 107573-17-1, is a synthetic compound that belongs to the class of peptides. It is composed of three amino acids: alanine, phenylalanine, and lysine, which are linked together in a specific sequence. This compound may exhibit properties typical of peptides, such as the ability to form hydrogen bonds, influence biological activity, and interact with various receptors or enzymes. The presence of fluoromethane suggests that it may have unique characteristics related to its fluorinated structure, potentially affecting its solubility, stability, and reactivity. Peptides like this one can play significant roles in biological systems, including acting as signaling molecules or influencing metabolic pathways. Additionally, the specific arrangement of amino acids can impart unique properties, such as increased hydrophobicity or the ability to form secondary structures. Overall, alanyl-phenylalanyl-lysine fluoromethane represents a complex interplay of chemical and biological characteristics that may be of interest in pharmaceutical and biochemical research.
Formula:C19H31FN4O4
InChI:InChI=1/C18H28N4O4.CH3F/c1-12(20)16(23)22-15(11-13-7-3-2-4-8-13)17(24)21-14(18(25)26)9-5-6-10-19;1-2/h2-4,7-8,12,14-15H,5-6,9-11,19-20H2,1H3,(H,21,24)(H,22,23)(H,25,26);1H3/t12-,14-,15-;/m0./s1
SMILES:C[C@@H](C(=N[C@@H](Cc1ccccc1)C(=N[C@@H](CCCCN)C(=O)O)O)O)N.CF
Synonyms:- Ala-phe-lys-CH2F
- L-alanyl-L-phenylalanyl-L-lysine - fluoromethane (1:1)
- Alanyl-phenylalanyl-lysine fluoromethane
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Found 1 products.
Alanyl-phenylalanyl-lysine fluoromethane
CAS:Controlled Product<p>Alanyl-phenylalanyl-lysine fluoromethane is a competitive inhibitor of the enzyme kallikrein. It binds to the active site of kallikrein and competes with the natural substrate peptidyl-piperidinium for binding, thereby inhibiting the activity of the enzyme. Alanyl-phenylalanyl-lysine fluoromethane has been shown to inhibit coagulation by blocking the activation of prothrombin and thrombin by kallikrein. This inhibition can be reversed by adding an anticoagulant such as heparin or hirudin. The biochemical assay used to measure this drug's effect on coagulation requires analysis using fluoroalkyl reagents, which are not suitable for use in human subjects.</p>Formula:C19H31FN4O4Purity:Min. 95%Molecular weight:398.47 g/mol
