CAS 23420-32-8
:Boc-Phe-Pro-OH
Description:
Boc-Phe-Pro-OH, also known as Boc-phenylalanine-proline hydroxyl, is a protected amino acid derivative commonly used in peptide synthesis. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, allowing for selective reactions without interfering with the amine. The phenylalanine (Phe) and proline (Pro) residues contribute to the molecule's structural and functional properties, influencing the conformation and stability of peptides in which they are incorporated. This compound is typically utilized in the synthesis of peptides due to its ability to facilitate the formation of peptide bonds while maintaining the integrity of the amino acid side chains. Its solubility in organic solvents and stability under various reaction conditions make it a valuable intermediate in organic synthesis and medicinal chemistry. Additionally, the presence of the hydroxyl group at the C-terminus can enhance the compound's reactivity and potential for further modifications. Overall, Boc-Phe-Pro-OH is an important building block in the field of peptide chemistry.
Formula:C19H26N2O5
InChI:InChI=1/C19H26N2O5/c1-19(2,3)26-18(25)20-14(12-13-8-5-4-6-9-13)16(22)21-11-7-10-15(21)17(23)24/h4-6,8-9,14-15H,7,10-12H2,1-3H3,(H,20,25)(H,23,24)
SMILES:CC(C)(C)OC(=NC(Cc1ccccc1)C(=O)N1CCCC1C(=O)O)O
Synonyms:- N-(tert-butoxycarbonyl)phenylalanylproline
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Found 4 products.
L-Proline, N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl-
CAS:Formula:C19H26N2O5Purity:97%Molecular weight:362.4201(S)-1-((S)-2-((tert-Butoxycarbonyl)amino)-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid
CAS:(S)-1-((S)-2-((tert-Butoxycarbonyl)amino)-3-phenylpropanoyl)pyrrolidine-2-carboxylic acidPurity:97%Molecular weight:362.43g/molBoc-Phe-Pro-OH
CAS:<p>Boc-Phe-Pro-OH is an opioid receptor agonist. It binds to the δ opioid receptors and activates them, which leads to analgesic effects. Boc-Phe-Pro-OH also has antibacterial properties and can be used for the treatment of bacterial infections. This compound may also have antiinflammatory properties that are mediated by its ability to inhibit prostaglandin synthesis. Boc-Phe-Pro-OH has been shown to possess a high affinity for the μ opioid receptor, but does not activate this receptor subtype.</p>Formula:C19H26N2O5Purity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:362.42 g/mol




