Search results for "Sialyl-Lewis X"

showing 9 items of 9 documents

Specific norovirus interaction with Lewis x and Lewis a on human intestinal inflammatory mucosa during refractory inflammatory bowel disease

2021

Inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), are progressive diseases affecting millions of people each year. Flare-ups during IBD result in severe mucosal alterations of the small intestine (in CD) and in the colon and rectum (in CD and UC).

0301 basic medicineCrohn’s diseaseMaleSeverity of Illness IndexInflammatory bowel diseasechemistry.chemical_compound0302 clinical medicineMedicineIntestinal MucosaCrohn's disease0303 health sciencesMiddle AgedImmunohistochemistryUlcerative colitisQR1-502HBGA3. Good healthmedicine.anatomical_structure030220 oncology & carcinogenesisImmunohistochemistry030211 gastroenterology & hepatologyFemalegut inflammationResearch ArticleAdultCA-19-9 Antigenmedicine.drug_classLewis X AntigenRectumMonoclonal antibodyMicrobiologydigestive systemVirusHost-Microbe BiologyYoung Adult03 medical and health sciencesAntigenHumansMolecular Biologyulcerative colitis030304 developmental biologybusiness.industryNorovirus[SDV.MHEP.HEG]Life Sciences [q-bio]/Human health and pathology/Hépatology and GastroenterologySialyl-Lewis AInflammatory Bowel Diseasesmedicine.diseasedigestive system diseasesSmall intestineGastrointestinal Tract030104 developmental biologySialyl-Lewis XchemistryinflammationImmunologybusiness[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
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Synthesis and biological activity of novel sialyl-lewisX conjugates

1996

Abstract Novel sialyl Lewis X conjugates have been synthesized and evaluated as inhibitors of E- and P-selectin mediated cell adhesion in cell culture assays. The most potent conjugate in the static inhibition assays exhibited a significant and dose-dependent pharmacological potency as inhibitor of the edotoxin-induced leukocyte adhesion to the endothelium of postcapillary venules in rats.

EndotheliumOrganic ChemistryClinical BiochemistryPharmaceutical ScienceBiological activityAdhesionBiochemistrychemistry.chemical_compoundSialyl-Lewis Xmedicine.anatomical_structurechemistryBiochemistryDrug DiscoverymedicineMolecular MedicinePotencyCell adhesionMolecular BiologyConjugateBioorganic & Medicinal Chemistry Letters
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Chemical and chemoenzymatic synthesis of glycopeptide selectin ligands containing sialyl Lewis X structures.

2010

GlycosylationGlycosylationChemistryStereochemistryOrganic ChemistryGlycopeptidesOligosaccharidesLigandsBiochemistryGlycopeptidechemistry.chemical_compoundSialyl-Lewis XSelectinsMolecular MedicineSialyl Lewis X AntigenMolecular BiologySelectinChembiochem : a European journal of chemical biology
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Synthesis of tumor-associated glycopeptide antigens.

2002

Carbohydrates and peptides linked together in glycoproteins constitute important components of the molecular communication between cells in multicellular organisms. Cell morphogenesis and tumorigenesis are accompanied by changes in the glycoprotein profiles of the outer cell membranes. Glycopeptide fragments of glycoproteins that have altered structures in tumor cells are of interest as tumor-associated antigens for the distinction between normal cells and tumor cells. In contrast to glycoproteins isolated from biological sources, synthetic glycopeptides are obtained in pure form and exactly specified structures. The methods developed for the synthesis of glycopeptides with tumor-associated…

GlycosylationStereochemistryClinical BiochemistryPharmaceutical ScienceOligosaccharidesBiochemistrychemistry.chemical_compoundLewis Blood Group AntigensDrug DiscoveryHumansAntigens Tumor-Associated CarbohydrateAntigens Viral TumorMolecular Biologychemistry.chemical_classificationCell morphogenesisOrganic ChemistryGlycopeptidesSialyl-Lewis AGlycopeptideSialic acidAmino acidSialyl-Lewis XchemistryBiochemistrySialic AcidsMolecular MedicineGlycoproteinBioorganicmedicinal chemistry
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Chemoenzymatic Synthesis of Functional Sialyl LewisX Mimetics with a Heteroaromatic Core

2014

Functional mimetics of the sialyl Lewis(X) tetrasaccharide were prepared by the enzymatic sialylation of a 1,3-diglycosylated indole and a glycosyl azide, which was subsequently transformed into a 1,4-diglycosylated 1,2,3-triazole, by using the trans-sialidase of Trypanosoma cruzi. These compounds inhibited the binding of E-, L-, and P-selectin-coated nanoparticles to polyacrylamide-bound sialyl-Lewis(X) -containing neighboring sulfated tyrosine residues (sTyr/sLe(X) -PAA) at low or sub-millimolar concentrations. Except for E-selectin, the mimetics showed higher activities than the natural tetrasaccharide.

Spectrometry Mass Electrospray IonizationStereochemistryProton Magnetic Resonance SpectroscopyTrypanosoma cruziMolecular Sequence DataNeuraminidaseOligosaccharidessaccharide mimeticsBiochemistryenzyme catalysisEnzyme catalysischemistry.chemical_compoundSulfationTetrasaccharideAnimalsGlycosylTyrosineCarbon-13 Magnetic Resonance SpectroscopySialyl Lewis X AntigenGlycoproteinsIndole testheterocyclesOrganic ChemistryMolecular Mimicrycell adhesionGeneral ChemistryFull Paperscarbohydrates (lipids)Sialyl-Lewis XchemistryCarbohydrate SequenceSelectinsAzideChemistry, an Asian Journal
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Oligosaccharide recognition by selectins: Synthesis and biological activity of multivalent sialyl lewis-X ligands

1995

Abstract Trivalent sialyl Lewis-X ligands 6–8 anchored onto flexible templates have been synthesized and evaluated as inhibitors of E-selectin and P-selectin mediated cell adhesion in cell culture assays and in vivo. Biological activities in vitro correlated with spacer length and lead to ligands with 3-fold (E-selectin) and 5-fold (P-selectin) improved receptor binding avidity per single tetrasaccharide moiety.

chemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryBiological activityOligosaccharideBiochemistrychemistry.chemical_compoundSialyl-Lewis XBiochemistryDrug DiscoveryMoietyTetrasaccharideAvidityCell adhesionSelectinTetrahedron
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(p-Sulfomethyl)phenylalanine as a mimic of O-sulfatyl-tyrosine in synthetic partial sequences of P-Selectin glycoprotein ligand 1 (PSGL-1)

2007

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.

chemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryPhenylalanineLigand (biochemistry)Peptide conjugateBiochemistrychemistry.chemical_compoundSialyl-Lewis XDrug DiscoverySide chainP-selectin glycoprotein ligand-1TyrosineGlycoproteinTetrahedron
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ChemInform Abstract: Synthesis of Tumor-Associated Glycopeptide Antigens

2010

Carbohydrates and peptides linked together in glycoproteins constitute important components of the molecular communication between cells in multicellular organisms. Cell morphogenesis and tumorigenesis are accompanied by changes in the glycoprotein profiles of the outer cell membranes. Glycopeptide fragments of glycoproteins that have altered structures in tumor cells are of interest as tumor-associated antigens for the distinction between normal cells and tumor cells. In contrast to glycoproteins isolated from biological sources, synthetic glycopeptides are obtained in pure form and exactly specified structures. The methods developed for the synthesis of glycopeptides with tumor-associated…

chemistry.chemical_classificationchemistry.chemical_compoundGlycosylationSialyl-Lewis XchemistryBiochemistryCell morphogenesisGeneral MedicineSialyl-Lewis AGlycoproteinGlycopeptideAmino acidSialic acidChemInform
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ChemInform Abstract: Chemical and Chemoenzymatic Synthesis of Glycopeptide Selectin Ligands Containing Sialyl Lewis X Structures

2010

chemistry.chemical_compoundSialyl-Lewis XChemistryStereochemistryGeneral MedicineSelectinGlycopeptideChemInform
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