Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/34882
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dc.contributor.authorLe Sann, C.-
dc.contributor.authorGower, M.-
dc.contributor.authorAbell, A.-
dc.date.issued2004-
dc.identifier.citationMini-Reviews in Medicinal Chemistry, 2004; 4(7):747-756-
dc.identifier.issn1389-5575-
dc.identifier.issn1875-5607-
dc.identifier.urihttp://hdl.handle.net/2440/34882-
dc.description.abstractInhibitors of varying potency have been developed for types I and II 3-dehydroquinate dehydratase (dehydroquinase), enzymes from the shikimate and quinate pathways that catalyse the dehydration of dehydroquinate to dehydroshikimate. These inhibitors have resulted from enzyme mechanistic studies and from the direct search for enzyme inhibitors with herbicidal, fungicidal or antimicrobial potential. This review discusses the design of the various inhibitors that have been produced so far and some structure-activity relationships. The majority of these inhibitors are based on dehydroquinate analogues, although some work has also been carried out on dehydroshikimate and bissulfonamides. Some discussion is also presented on advances in the synthesis of these types of compounds.-
dc.description.statementofresponsibilityChristine Le Sann, Mary A. Gower and Andrew D. Abell-
dc.description.urihttp://www.bentham.org/mrmc/ContentAbstract_body.htm-
dc.language.isoen-
dc.publisherBentham Science Publishers Ltd.-
dc.subjectStreptomyces coelicolor-
dc.subjectSalmonella typhimurium-
dc.subjectMycobacterium tuberculosis-
dc.subjectAspergillus nidulans-
dc.subjectHydro-Lyases-
dc.subjectEnzyme Inhibitors-
dc.subjectMolecular Structure-
dc.subjectStructure-Activity Relationship-
dc.subjectSubstrate Specificity-
dc.titleInhibitors of types I and II dehydroquinase-
dc.typeJournal article-
pubs.publication-statusPublished-
dc.identifier.orcidAbell, A. [0000-0002-0604-2629]-
Appears in Collections:Aurora harvest 6
Chemistry publications

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