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Abstract
© 2016 The Royal Society of Chemistry. The synthesis of analogues of the potent N-acetylhexosaminidase inhibitor, PUGNAc, are described. These compounds were assayed against a set of biologically important N-acetyl-d-glucosaminidases and were found to vary in both potency and selectivity.
Original language | English |
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Pages (from-to) | 3193-3197 |
Number of pages | 5 |
Journal | Organic and Biomolecular Chemistry |
Volume | 14 |
Issue number | 12 |
DOIs | |
Publication status | Published - 23 Feb 2016 |
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Dive into the research topics of 'Modifying the phenyl group of PUGNAc: Reactivity tuning to deliver selective inhibitors for N-acetyl-d-glucosaminidases'. Together they form a unique fingerprint.Projects
- 1 Finished
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Using Genetic Tools to Study Helicobacter Pylori & Persistence
Debowski, A. (Investigator 01)
NHMRC National Health and Medical Research Council
1/01/14 → 28/02/18
Project: Research