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dc.contributor.authorRossiter, S.
dc.contributor.authorSmith, C.L.
dc.contributor.authorMalaki, M.
dc.contributor.authorNandi, M.
dc.contributor.authorGill, H.
dc.contributor.authorLeiper, J.M.
dc.contributor.authorVallance, P.
dc.contributor.authorSelwood, D.L.
dc.date.accessioned2008-11-18T10:08:22Z
dc.date.available2008-11-18T10:08:22Z
dc.date.issued2005
dc.identifier.citationRossiter , S , Smith , C L , Malaki , M , Nandi , M , Gill , H , Leiper , J M , Vallance , P & Selwood , D L 2005 , ' Selective substrate-based inhibitors of mammalian dimethylarginine dimethylaminohydrolase ' , Journal of Medicinal Chemistry , vol. 48 , no. 14 , pp. 4670-4678 . https://doi.org/10.1021/jm050187a
dc.identifier.issn0022-2623
dc.identifier.otherdspace: 2299/2619
dc.identifier.otherORCID: /0000-0003-3822-0028/work/142009573
dc.identifier.urihttp://hdl.handle.net/2299/2619
dc.descriptionOriginal article can be found at: http://pubs.acs.org/journal/jmcmar Copyright American Chemical Society DOI: 10.1021/jm050187a [Full text of this article is not available in the UHRA]
dc.description.abstractThe enzyme DDAH metabolizes methylarginines that are inhibitors of nitric oxide synthase (NOS). Substrate-based inhibitors of mammalian DDAH have been synthesized, with optimization to give selective inhibition of DDAH with no significant direct effect on NOSs. These are the first examples of reversible DDAH inhibitors with significant activity and selectivity. In vivo administration increases plasma ADMA levels, giving proof of concept that these inhibitors can be used to probe the physiological effects of DDAH inhibition, with potential for pharmaceutical use of DDAH inhibitors in diseases where excess NO production is implicated.en
dc.language.isoeng
dc.relation.ispartofJournal of Medicinal Chemistry
dc.titleSelective substrate-based inhibitors of mammalian dimethylarginine dimethylaminohydrolaseen
dc.contributor.institutionDepartment of Pharmacy
dc.contributor.institutionPsychopharmacology, Drug Misuse and Novel Psychoactive Substances Unit
dc.contributor.institutionCentre for Research in Mechanisms of Disease and Drug Discovery
dc.contributor.institutionNatural Product Chemistry and Drug Design
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.contributor.institutionSchool of Life and Medical Sciences
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.1021/jm050187a
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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