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dc.contributor.authorMoorhouse, Adam D.
dc.contributor.authorSpiteri, Christian
dc.contributor.authorSharma, Pallavi
dc.contributor.authorZloh, Mire
dc.contributor.authorMoses, John E.
dc.date.accessioned2013-04-25T09:20:05Z
dc.date.available2013-04-25T09:20:05Z
dc.date.issued2011
dc.identifier.citationMoorhouse , A D , Spiteri , C , Sharma , P , Zloh , M & Moses , J E 2011 , ' Targeting glycolysis : a fragment based approach towards bifunctional inhibitors of hLDH-5 ' , Chemical Communications , vol. 47 , no. 1 , pp. 230-2 . https://doi.org/10.1039/c0cc01166e
dc.identifier.issn1364-548X
dc.identifier.otherPURE: 1457397
dc.identifier.otherPURE UUID: ea8afce3-c322-4024-983b-6b9de00227e9
dc.identifier.otherPubMed: 20676418
dc.identifier.otherScopus: 78649848379
dc.identifier.urihttp://hdl.handle.net/2299/10548
dc.description.abstracthLDH-5 has emerged as a promising target for anti-glycolytic cancer chemotherapy. Here we report a first generation of bifunctional inhibitors, which show promising activity against hLDH-5.en
dc.format.extent3
dc.language.isoeng
dc.relation.ispartofChemical Communications
dc.titleTargeting glycolysis : a fragment based approach towards bifunctional inhibitors of hLDH-5en
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionHealth & Human Sciences Research Institute
dc.contributor.institutionDepartment of Pharmacy
dc.contributor.institutionMedicinal and Analytical Chemistry
dc.description.statusPeer reviewed
rioxxterms.versionofrecordhttps://doi.org/10.1039/c0cc01166e
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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