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Detalle de: Tetrahydrobenzothiophene derivatives: conformationally restricted inhibitors of type II dehydroquinase.

Title Tetrahydrobenzothiophene derivatives: conformationally restricted inhibitors of type II dehydroquinase.
Abstract

Restriction is good for inhibition! Tetrahydrobenzothiophene-derived rigid mimics of the type II dehydroquinase (DHQ2)-catalyzed reaction intermediate are reported. These derivatives fix the interaction with the tyrosine, the base that initiates the enzymatic reaction, in an inappropriate orientation for catalysis. Two competitive inhibitors in the series, 2-propenyl derivative 5 e and 2-cyclopropylethyl compound 5 i (shown), were crystallized in complex with DHQ2 from Helicobacter pylori, and the X-ray structures were determined at 1.95 Å and 1.85 Å, respectively.

Apa Reference Paz, S., Tizón, L., Otero, J. M., Llamas‐Saiz, A. L., Fox, G. C., van Raaij, M. J., Lamb, H., Hawkins, A. R., Lapthorn, A. J., Castedo, L., & González‐Bello, C. (2010). Tetrahydrobenzothiophene Derivatives: Conformationally Restricted Inhibitors of Type II Dehydroquinase. ChemMedChem, 6(2), 266–272. Portico. 10.1002/cmdc.201000343
Doi 10.1002/cmdc.201000343
Publication Date 10 Nov 2010
Publication Type Article
Researcher Mark van Raaij
Ontology Molecular flexibility, Drug Discovery and design
Research Groups Structural Biology of Virus Proteins
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