6533b839fe1ef96bd12a640e

RESEARCH PRODUCT

(p-Sulfomethyl)phenylalanine as a mimic of O-sulfatyl-tyrosine in synthetic partial sequences of P-Selectin glycoprotein ligand 1 (PSGL-1)

Horst KunzHolger Herzner

subject

chemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryPhenylalanineLigand (biochemistry)Peptide conjugateBiochemistrychemistry.chemical_compoundSialyl-Lewis XDrug DiscoverySide chainP-selectin glycoprotein ligand-1TyrosineGlycoprotein

description

Abstract Fmoc- l -( p -sulfomethyl)phenylalanine, a bioisosteric mimic of acid-sensitive O -sulfatyl tyrosine, was synthesized from l -tyrosine according to a novel route. Partial sequences of the recognition site of P-Selectin glycoprotein ligand 1 (PSGL-1), which contain (sulfomethyl)phenylalanine were synthesized on solid-phase. By fragment condensation, a sialyl Lewis x peptide conjugate containing a (sulfomethyl)phenylalanine mimic of O -sulfatyl tyrosine was prepared without destruction of the acid-sensitive fucoside bond within the saccharide side chain. Compounds of this type are of interest as sufficiently acid-stable potential inhibitors of P-Selectin in inflammatory processes.

https://doi.org/10.1016/j.tet.2007.03.028