52083-48-4Relevant academic research and scientific papers
1H NMR study of the complexation of aromatic drugs with dimethylxanthine derivatives
Hernandez Santiago,Gonzalez Flores,Rosas Castilla,Cervantes Tavera,Gutierrez Perez,Khomich,Ovchinnikov,Parkes,Evstigneev
, p. 139 - 145 (2012)
With an aim of searching efficient interceptors of aromatic drugs, the self- and hetero-association of dimethylxanthine derivatives with different structures, selected according to Strategy 1 (variation of the position of methyl groups) and Strategy 2 (variation of the length of (CH2) nCOOH group), with aromatic drug molecules: Ethidium Bromide, Proflavine and Daunomycin, were studied using 1H NMR spectroscopy. It was found that the association proceeds in a form of stacking-type complexation and its energetics is relatively independent on the structure of the dimethylxanthines. However, on average, the dimethylxanthines possess higher hetero-association constant and, hence, higher interceptor ability as compared to the trimethylxanthine, Caffeine, used during the past two decades as a typical interceptor molecule.
Antigen, antiserum and immunoassay for theophylline
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, (2008/06/13)
By injecting a host animal with a member of a particular group of antigens [a theophylline-(7)-alkanecarboxylic acid covalently bonded to an immunogenic carrier (IGC) via the carboxyl group], antibodies, advantageously employed in determining small amounts of theophylline in biological liquids by immunoassay methods, are obtained.
