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Bioorg Med Chem ; 8(3): 657-64, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10732983

ABSTRACT

Several C-9 modified N-acetylneuraminic acid derivatives have been synthesised and evaluated as substrates of N-acetylneuraminic acid aldolase. Simple C-9 acyl or ether modified derivatives of N-acetylneuraminic acid were found to be accepted as substrates by the enzyme, albeit being transformed more slowly than Neu5Ac itself. 1H NMR spectroscopy was used to evaluate the extent of the enzyme catalysed transformation of these compounds. Interestingly, the chain-extended Neu5Ac derivative 16 is not a substrate for N-acetylneuraminate lyase and behaves as an inhibitor of the enzyme.


Subject(s)
N-Acetylneuraminic Acid/chemistry , Oxo-Acid-Lyases/metabolism , Bacterial Proteins , Binding Sites , Escherichia coli/enzymology , Kinetics , Membranes, Artificial , Molecular Probes , N-Acetylneuraminic Acid/analogs & derivatives , N-Acetylneuraminic Acid/chemical synthesis , Oxo-Acid-Lyases/antagonists & inhibitors , Oxo-Acid-Lyases/chemistry , Substrate Specificity
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