The conformationally restricted tripeptides HCO-L-Met-Xxx-L-Phe-OMe [where Xxx is L (D)-Iva, -(alphaMe)Val or -(alphaMe)Phe] were synthesized and tested for their beta-glucosaminidase release activity. The [L-(alphaMe)Val]2- and [L-(alphaMe)Leu]2- analogues turned out to be the most active compounds examined. The positive effects induced by increasing side-chain hydrophobicity and by the L-chirality of the Xxx residue on peptide-receptor interactions are discussed.

Backbone Modified Formyl-methionyl Tripeptide Chemoattractants

FORMAGGIO, FERNANDO;TONIOLO, CLAUDIO;
1993

Abstract

The conformationally restricted tripeptides HCO-L-Met-Xxx-L-Phe-OMe [where Xxx is L (D)-Iva, -(alphaMe)Val or -(alphaMe)Phe] were synthesized and tested for their beta-glucosaminidase release activity. The [L-(alphaMe)Val]2- and [L-(alphaMe)Leu]2- analogues turned out to be the most active compounds examined. The positive effects induced by increasing side-chain hydrophobicity and by the L-chirality of the Xxx residue on peptide-receptor interactions are discussed.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/2523461
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