Boc-Phe-Leu-Phe-Leu-Phe-OH, with the CAS number 73572-58-4, is a synthetic peptide that features a sequence of amino acids, specifically phenylalanine (Phe) and leucine (Leu), with a tert-butyloxycarbonyl (Boc) protecting group on the N-terminus. This compound is characterized by its hydrophobic nature due to the presence of aromatic and aliphatic side chains, which can influence its solubility and interaction with biological membranes. The Boc group serves as a protective moiety that facilitates peptide synthesis by preventing unwanted reactions at the amino group. Peptides like Boc-Phe-Leu-Phe-Leu-Phe-OH are often studied for their potential biological activities, including their roles in signaling pathways and as potential therapeutic agents. Additionally, the structural arrangement of the amino acids can affect the peptide's conformation, stability, and binding affinity to various targets. Overall, this compound exemplifies the complexity and versatility of peptide chemistry in both research and pharmaceutical applications.

Boc-Phe-Leu-Phe-Leu-Phe-OH

73572-58-4: Boc-Phe-Leu-Phe-Leu-Phe-OH, with the CAS number 73572-58-4, is a synthetic peptide that features a sequence of amino acids, specifically phenylalanine (Phe) and leucine (Leu), with a tert-butyloxycarbonyl (Boc) protecting group on the N-terminus. This compound is characterized by its hydrophobic nature due to the presence of aromatic and aliphatic side chains, which can influence its solubility and interaction with biological membranes. The Boc group serves as a protective moiety that facilitates peptide synthesis by preventing unwanted reactions at the amino group. Peptides like Boc-Phe-Leu-Phe-Leu-Phe-OH are often studied for their potential biological activities, including their roles in signaling pathways and as potential therapeutic agents. Additionally, the structural arrangement of the amino acids can affect the peptide's conformation, stability, and binding affinity to various targets. Overall, this compound exemplifies the complexity and versatility of peptide chemistry in both research and pharmaceutical applications.

A competitive antagonist of the binding of For-Met-Leu-Phe-OH to neutrophils.

<p>Boc-Phe-Leu-Phe-Leu-Phe is a chemotactic peptide antagonist that inhibits the release of peptide leukotrienes induced by FMLP.</p>

Boc-Phe-Leu-Phe-Leu-Phe

<p>Boc-Phe-Leu-Phe-Leu-Phe-OH is a cyclase inhibitor that binds to the receptor molecule, which is part of the signaling pathway of chemotactic activity. It has been shown in vitro to inhibit the proliferation of diabetic retinopathy cells and to have chemotactic activity for polymorphonuclear leucocytes. Boc-Phe-Leu-Phe-Leu-Phe-OH is also an antagonist of chelerythrine, which is a potent activator of hl60 cells and a potent inhibitor of microbial infections.</p>

CAS 73572-58-4

Boc-Phe-Leu-Phe-Leu-Phe-OH

Boc-Phe-Leu-Phe-Leu-Phe-OH

Ref: 01-4007828

Boc-Phe-Leu-Phe-Leu-Phe

Ref: TM-TP2924

Boc-Phe-Leu-Phe-Leu-Phe-OH

Ref: 3D-FB111222