Issue 30, 2012

Synthesis of selective inhibitors against V. cholerae sialidase and human cytosolic sialidase NEU2

Abstract

Sialidases or neuraminidases catalyze the hydrolysis of terminal sialic acid residues from sialyl oligosaccharides and glycoconjugates. Despite successes in developing potent inhibitors specifically against influenza virus neuraminidases, the progress in designing and synthesizing selective inhibitors against bacterial and human sialidases has been slow. Guided by sialidase substrate specificity studies and sialidase crystal structural analysis, a number of 2-deoxy-2,3-dehydro-N-acetylneuraminic acid (DANA or Neu5Ac2en) analogues with modifications at C9 or at both C5 and C9 were synthesized. Inhibition studies of various bacterial sialidases and human cytosolic sialidase NEU2 revealed that Neu5Gc9N32en and Neu5AcN39N32en are selective inhibitors against V. cholerae sialidase and human NEU2, respectively.

Graphical abstract: Synthesis of selective inhibitors against V. cholerae sialidase and human cytosolic sialidase NEU2

Supplementary files

Article information

Article type
Paper
Submitted
16 fev 2012
Accepted
08 mai 2012
First published
08 mai 2012

Org. Biomol. Chem., 2012,10, 6112-6120

Synthesis of selective inhibitors against V. cholerae sialidase and human cytosolic sialidase NEU2

Z. Khedri, Y. Li, H. Cao, J. Qu, H. Yu, M. M. Muthana and X. Chen, Org. Biomol. Chem., 2012, 10, 6112 DOI: 10.1039/C2OB25335F

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