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dc.contributor.author Mirzahosseini, Arash
dc.contributor.author Noszál, Béla
dc.date.accessioned 2014-12-20T20:20:24Z
dc.date.available 2014-12-20T20:20:24Z
dc.date.issued 2014
dc.identifier 84897823651
dc.identifier.citation pagination=184-192; journalVolume=95C; journalTitle=JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/866
dc.identifier.uri doi:10.1016/j.jpba.2014.02.023
dc.description.abstract Cysteamine, cysteine, homocysteine, their homodisulfides and 9 related compounds were studied by 1H NMR-pH titrations and case-tailored evaluation methods. The resulting acid-base properties are quantified in terms of 33 macroscopic and 62 microscopic protonation constants and the concomitant 16 interactivity parameters, providing thus the first complete microspeciation of this vitally important family of biomolecules. The species- and site-specific basicities are interpreted by means of inductive and hydrogen-bonding effects through various intra- and intermolecular comparisons. The pH-dependent distribution of the microspecies is depicted. The thiolate basicities determined this way provide exclusive means for the prediction of thiolate oxidizabilities, a key parameter to understand and influence oxidative stress at the molecular level.
dc.relation.ispartof urn:issn:0731-7085
dc.title The species- and site-specific acid-base properties of biological thiols and their homodisulfides.
dc.type Journal Article
dc.date.updated 2014-12-20T20:19:32Z
dc.language.rfc3066 en
dc.identifier.mtmt 2569444
dc.identifier.wos 000336558600025
dc.identifier.pubmed 24675073
dc.contributor.department SE/GYTK/Gyógyszerészi Kémiai Intézet
dc.contributor.institution Semmelweis Egyetem


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