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High performance liquid chromatography-electrochemistry-electrospray ionization mass spectrometry (HPLC/EC/ESI-MS) for detection and characterization of roscovitine oxidation products

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dc.title High performance liquid chromatography-electrochemistry-electrospray ionization mass spectrometry (HPLC/EC/ESI-MS) for detection and characterization of roscovitine oxidation products en
dc.contributor.author Karady, Michal
dc.contributor.author Novák, Ondřej
dc.contributor.author Horna, Aleš
dc.contributor.author Strnad, Miroslav
dc.contributor.author Doležal, Karel
dc.relation.ispartof Electroanalysis
dc.identifier.issn 1040-0397 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2011
utb.relation.volume 23
utb.relation.issue 12
dc.citation.spage 2898
dc.citation.epage 2905
dc.type article
dc.language.iso en
dc.publisher Wiley-Blackwell en
dc.identifier.doi 10.1002/elan.201100383
dc.relation.uri http://onlinelibrary.wiley.com/doi/10.1002/elan.201100383/full
dc.subject Electrochemistry en
dc.subject Mass spectrometry en
dc.subject Oxidation en
dc.subject R-roscovitine en
dc.description.abstract On-line LC-EC/ESI-MS has been established as a fast and simple method to mimic some types of oxidation reaction of various drugs and to study the formation and structure of the resulting products. This technique has been applied to a 2,6,9-trisubstituted purine, R-roscovitine, which is known to be an inhibitor of some cyclin-dependent kinases (CDKs) and a potential anticancer drug. Oxidation of R-roscovitine in an electrochemical cell (EC), operated under various conditions, resulted in appearance of 6 major products. These were further analyzed by high-resolution mass spectrometry, their structures were elucidated by accurate mass measurement and compared to previously identified R-roscovitine in vitro/in vivo metabolites. Although none of the observed products was structurally identical to those identified previously in vitro/in vivo, all of them, except for the methoxylated products, resembled similarity due to appearing through the same reaction type. R-roscovitine in the EC cell underwent N-dealkylation of the isopropyl moiety, hydroxylation of the aromatic side-chain, dihydroxylation, methoxylation and dimer formation. The hydroxylation product was identified as Olomoucine II, a R-roscovitine derivative, which displays 10-times higher CDK-inhibiting activity than R-roscovitine and the occurrence of which, as R-roscovitine product, has not yet been observed in vitro/in vivo. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. en
utb.faculty University Institute
dc.identifier.uri http://hdl.handle.net/10563/1002595
utb.identifier.rivid RIV/70883521:28610/12:43866427!RIV13-MSM-28610___
utb.identifier.obdid 43866535
utb.identifier.scopus 2-s2.0-83355177556
utb.identifier.wok 000298063500018
utb.identifier.coden ELANE
utb.source j-scopus
dc.date.accessioned 2012-02-10T13:15:10Z
dc.date.available 2012-02-10T13:15:10Z
utb.ou Centre of Polymer Systems
utb.contributor.internalauthor Horna, Aleš
utb.fulltext.affiliation Michal Karady,a Ondřej Novák,a Aleš Horna ,c, d Miroslav Strnad,a, b Karel Doležal*a, b a Laboratory of Growth Regulators, Palacky University and Institute of Experimental Botany ASCR, Šlechtitelů 11, 783 71, Olomouc, Czech Republic b Centre of the Region Han for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Šlechtitelů 11, CZ 783 71, Olomouc, Czech Republic c RADANAL Ltd., Okružní 613, Pardubice, 530 03, Czech Republic d Tomas Bata University in Zln, University Institute, Food Research Centre, Mostní 539, CZ-760 01 Zln, Czech Republic *e-mail: karel.dolezal@upol.cz
utb.fulltext.dates Received: July 19, 2011 Accepted: September 28, 2011
utb.fulltext.sponsorship This work was supported by the Czech Ministry of Education (MSM 6198959216), and Grant No. ED0007/01/01 from the Centre of the Region Han for Biotechnological and Agricultural Research
utb.fulltext.projects MSM 6198959216
utb.fulltext.projects ED0007/01/01
utb.fulltext.faculty University Institute
utb.fulltext.ou Food Research Centre
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