Zobrazit minimální záznam

dc.contributor.authorKuča, Kamil
dc.contributor.authorHrabinová, Martina
dc.contributor.authorJun, Daniel
dc.contributor.authorMusílek, Kamil
dc.contributor.authorPenhaker, Marek
dc.contributor.authorKrejcar, Ondřej
dc.contributor.authorSoukup, Ondřej
dc.date.accessioned2015-10-30T14:50:53Z
dc.date.available2015-10-30T14:50:53Z
dc.date.issued2015
dc.identifier.citationMedicinal Chemistry. 2015, vol. 11, issue 7, p. 683-686.cs
dc.identifier.issn1573-4064
dc.identifier.issn1875-6638
dc.identifier.urihttp://hdl.handle.net/10084/110528
dc.descriptionPubMed ID: 25845909cs
dc.description.abstractOxime K203 seems to be the most promising oxime in case of reactivation of tabuninhibited acetylcholinesterase (AChE). Although it was originally developed for treatment of tabun intoxications, it is able to reactivate cholinesterases inhibited by other nerve agents. This study is aimed at the evaluation of its potency in vitro against other nerve agents. For this purpose, sarin, tabun, cyclosarin, soman, VX, Russian VX and DFP were selected as members of the nerve agent family to check its universality. At high concentrations (10-3 M), oxime K203 reached promising reactivation activity. At low concentrations, relevant for human use (10-5 M), promising reactivation potency was obtained only with tabun. In conclusion, oxime K203 reactivates other nerve agents-inhibited cholinesterases, however its broad-spectrum reactivation is limited at high, for human not attainable, concentrations only. - See more at: http://www.eurekaselect.com/130155/article#sthash.TXpENEt9.dpufcs
dc.language.isoencs
dc.publisherBentham Sciencecs
dc.relation.ispartofseriesMedicinal Chemistrycs
dc.relation.urihttp://dx.doi.org/10.2174/1573406411666150407154204cs
dc.titleUniversality of oxime K203 for reactivation of nerve agent-inhibited AChEcs
dc.typearticlecs
dc.identifier.doi10.2174/1573406411666150407154204
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume11cs
dc.description.issue7cs
dc.description.lastpage686cs
dc.description.firstpage683cs
dc.identifier.wos000361825400011


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