Synthesis and biological activity of a conformationally constrained chemotactic gamma-lactam formyl tetrapeptide.
Giorgio Cavicchioni, Angela Breveglieri, Eva Reali, Susanna Spisani
Abstract
Giorgio Cavicchioni, Angela Breveglieri, Eva Reali, Susanna Spisani
Abstract
The synthesis and biological activity on human neutrophils of for-Met-(gamma-lactam)-Leu-Phe-OMe [fM(gamma l)LP-OMe], an analogue of the chemotactic fMLP-OMe, are reported. The tetrapeptide evidences chemotactic activity as well as superoxide anion production and lysozyme release, although with lower efficacy when compared with the parent tripeptide.
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The synthesis and biological activity on human neutrophils of for-Met-(gamma-lactam)-Leu-Phe-OMe [fM(gamma l)LP-OMe], an analogue of the chemotactic fMLP-OMe, are reported. The tetrapeptide evidences chemotactic activity as well as superoxide anion production and lysozyme release, although with lower efficacy when compared with the parent tripeptide.
Key concepts: Tetrapeptide, Tripeptide, Chemotaxis, Lactam, Superoxide, Chemistry, Biological activity, Stereochemistry