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Bioorg Med Chem Lett ; 10(19): 2197-200, 2000 Oct 02.
Article in English | MEDLINE | ID: mdl-11012028

ABSTRACT

In a program directed towards the design and synthesis of mimics of ganglioside GM1, the NeuAc recognition domain was replaced by simple hydroxy acids, and the affinity of the new ligands to the cholera toxin was determined by fluorescence spectroscopy. The (R)-lactic acid derivative 4 was found to display the highest affinity of the series (KD = 190 microM).


Subject(s)
Cholera Toxin/metabolism , G(M1) Ganglioside/analogs & derivatives , G(M1) Ganglioside/chemical synthesis , G(M1) Ganglioside/metabolism , Molecular Mimicry , Receptors, Cell Surface/metabolism , G(M1) Ganglioside/chemistry , Molecular Structure , Receptors, Cell Surface/chemistry , Sialic Acids/chemistry , Spectrometry, Fluorescence
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