Publication | Closed Access
Di-, Tri-, and Tetravalent Dendritic Galabiosides That Inhibit Hemagglutination by <i>Streptococcus suis</i> at Nanomolar Concentration
100
Citations
25
References
1997
Year
Bioorganic ChemistryMicrobial PathogensGlycobiologyBacterial PathogensDendritic GalabiosidesMedical MicrobiologyNanomolar ConcentrationSoluble CompoundsTetravalent Dendritic GalabiosidesAntimicrobial ResistanceAntimicrobial Drug DiscoveryBiochemistryInhibit HemagglutinationBioconjugationAntibacterial AgentAntimicrobial CompoundClinical MicrobiologyBiomolecular EngineeringAntimicrobial SusceptibilityNatural SciencesBiotechnologyMicrobiologyMedicineMonomeric Galabiosides
Galabiose (Galα1-4Gal) derivatives were coupled to carrier molecules having mono-, di-, tri-, and tetrameric functionalities, thus creating mono- to tetravalent dendritic galabiosides (1−9). The di- to tetravalent galabiosides were several hundred times more efficient than the monomeric galabiosides in inhibiting hemagglutination by the Gram-positive bacterium Streptococcus suis, resulting in complete inhibition at low nanomolar concentrations. This is unprecedented in the field of inhibition of bacterial adhesion by soluble compounds.
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