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Pharmazie ; 61(12): 1019-21, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17283660

ABSTRACT

Products of the aerobic visible-light-promoted riboflavin-sensitised photooxidation of the sympathomimetic drug isoproterenol were identified by means of HPLC and spectrophotometric techniques. The oxidative process, mediated by superoxide radical anion, generates N-isopropylaminochrome as a main photoproduct with a quantum yield of 0.15. In parallel, the photodecomposition of riboflavin is prevented in the presence of isoproterenol. A reaction scheme for the photooxidation pathway of isoproterenol is proposed in analogy to former reports for related compounds.


Subject(s)
Adrenergic beta-Agonists/chemistry , Adrenergic beta-Agonists/radiation effects , Isoproterenol/chemistry , Isoproterenol/radiation effects , Photosensitizing Agents/chemistry , Riboflavin/chemistry , Algorithms , Chromatography, High Pressure Liquid , Magnetic Resonance Spectroscopy , Oxidation-Reduction , Photochemistry , Photolysis , Spectrophotometry, Ultraviolet
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