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A prodrug approach for improving antituberculosis activity of potent Mycobacterium tuberculosis type II dehydroquinase inhibitors.

Universidad De Santiago De Compostela

Synthesis and biological evaluation of new nanomolar competitive inhibitors of Helicobacter pylori type II dehydroquinase. Structural details of the role of the aromatic moieties with essential residues.

Universidad De Santiago De Compostela

Crystal structures of Helicobacter pylori type II dehydroquinase inhibitor complexes: new directions for inhibitor design.

University Of Glasgow

Exploring the water-binding pocket of the type II dehydroquinase enzyme in the structure-based design of inhibitors.

Universidad De Santiago De Compostela

In silico fragment-based drug design with SEED.

University Of Z£Rich