Title : Synthesis and Biological Evaluation of Non-Hydrolizable 1,2,3-Triazole Linked Sialic Acid Derivatives as Neuraminidase Inhibitors.

Pub. Date : 2009 Jun

PMID : 24223493






3 Functional Relationships(s)
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1 Synthesis and Biological Evaluation of Non-Hydrolizable 1,2,3-Triazole Linked Sialic Acid Derivatives as Neuraminidase Inhibitors. N-Acetylneuraminic Acid neuraminidase 1 Homo sapiens
2 Our approach is to generate non-natural N-glycosides of sialic acid that are resistant to neuraminidase catalyzed hydrolysis as opposed to the natural O-glycosides. N-Acetylneuraminic Acid neuraminidase 1 Homo sapiens
3 These novel sialic acid derivatives were then evaluated as potential neuraminidase inhibitors using a 96-well plate fluorescence assay; micromolar IC50 values were observed, comparable to the known sialidase inhibitor Neu5Ac2en. N-Acetylneuraminic Acid neuraminidase 1 Homo sapiens