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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/34890
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dc.contributor.authorAbell, A.-
dc.contributor.authorNabbs, B.-
dc.date.issued2001-
dc.identifier.citationBioorganic and Medicinal Chemistry, 2001; 9(3):621-628-
dc.identifier.issn0968-0896-
dc.identifier.issn1464-3391-
dc.identifier.urihttp://hdl.handle.net/2440/34890-
dc.description.abstractN-Acyl and N-sulfonylhydroxymetyhylpyrroles have been synthesised and shown to inhibit α-chymotrypsin. A hydrophobic group in the N-substituent has been shown to be required for activity.-
dc.description.statementofresponsibilityAndrew D. Abell, and Brent K. Nabbs-
dc.description.urihttp://www.sciencedirect.com/science/journal/09680896-
dc.language.isoen-
dc.publisherPergamon-Elsevier Science Ltd-
dc.rightsCopyright © 2001 Elsevier Science Ltd. All rights reserved.-
dc.source.urihttp://dx.doi.org/10.1016/s0968-0896(00)00274-1-
dc.subjectAnimals-
dc.subjectCattle-
dc.subjectPyrroles-
dc.subjectChymotrypsin-
dc.subjectSerine Proteinase Inhibitors-
dc.subjectStructure-Activity Relationship-
dc.subjectKinetics-
dc.titleRing-deactivated hydroxymethylpyrroles as inhibitors of α-chymotrypsin-
dc.title.alternativeRing-deactivated hydroxymethylpyrroles as inhibitors of alpha-chymotrypsin-
dc.typeJournal article-
dc.identifier.doi10.1016/S0968-0896(00)00274-1-
pubs.publication-statusPublished-
dc.identifier.orcidAbell, A. [0000-0002-0604-2629]-
Appears in Collections:Aurora harvest
Chemistry publications

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