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dc.contributor.authorThoithi, Grace N.
dc.contributor.authorSchepdael, Ann Van
dc.contributor.authorBusson, Roger
dc.contributor.authorJanssen, Gerard
dc.contributor.authorAerschot, Arthur Van
dc.contributor.authorHerdewijn, Piet
dc.contributor.authorRoets, Eugene
dc.contributor.authorHoogmartens, Jos
dc.date.accessioned2013-02-22T06:50:15Z
dc.date.issued2000
dc.identifier.citationNucleosides & nucleotides and Nucleic acids, 19(1&2), 189-203 (2000)en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/10689
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/10772709
dc.description.abstractLiquid chromatography was used to follow the degradation of hexopyranosylated cytosine nucleosides in buffers of acid, neutral and alkaline pH and of constant ionic strength, The compounds were found to degrade by hydrolysis to cytosine and/or by deamination to the corresponding uracil nucleosides. Degradation in acid is influenced by the number of sugar hydroxyl groups, presence of sugar double bonds and the type of anomer. Stability of some of the compounds was compared with that of related thymine nucleosides. Temperature studies support a unimolecular mechanism of hydrolysis at pH 1.22.en
dc.language.isoenen
dc.titleInvestigation of the kinetics of degradation of hexopyranosylated cytosine nucleosides using liquid chromatographyen
dc.typeArticleen
local.embargo.terms6 monthsen
local.publisherDepartment of Pharmaceuucal Chemistry, faculty of Pharmacy, University of Nairobien
local.publisher• Katholieke Universiteit Leuven, Laboratorium voor Parmaceutische Chemie en Analyse van Geneesmiddelen, Paculteit Farmaceutische Wetenschappen, Van Evenstraaten


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