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- W2017384596 abstract "Potential antibiotics: The substitution of either the pro-R or pro-S hydrogen of the 3-dehydroquinic acid, the natural substrate of type II dehydroquinase, by a group (R) that is able to interact with the base responsible for enzymatic catalysis, tyrosine, is used as a strategy for the development of reversible competitive inhibitors of this enzyme. Synthesised compounds were also subjected to molecular modelling studies to investigate their binding mode. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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- W2017384596 title "2-Substituted-3-Dehydroquinic Acids as Potent Competitive Inhibitors of Type II Dehydroquinase" @default.
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