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Electrooxidation of Some Methylxanthines known as Antagonists of Adenosine Receptors

机译:一些甲基黄嘌呤被称为腺苷受体拮抗剂的电氧化

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摘要

The electrochemical oxidation of 1,7-dimethylxanthine and 1,3,7-trimethyl xanthine,well known antagonist of adenosine receptors,has been studied in phosphate buffers of pH 2.8-10.0.The oxidation of both the xanthines occurred in a single 4e~-,4H~+ process.The presence of methyl group in these compounds at position 7 has been found responsible for shifting the peak potential of these compounds by greater than 400 mV more positive than xanthine.The kinetics of the UV adsorbing intermediate generated during oxidation has also been studied and it is found that the decay of the intermediate occursr in a pseudo-first order reaction.The products of the oxidation have been separated and characterised for both the compounds,and a tentative mechanism for the oxidation has also been suggested.
机译:在pH 2.8-10.0的磷酸盐缓冲液中研究了众所周知的腺苷受体拮抗剂1,7-二甲基黄嘌呤和1,3,7-三甲基黄嘌呤的电化学氧化。两种黄嘌呤的氧化都发生在单个4e〜 -,4H〜+过程。已发现这些化合物在7位上存在甲基,导致这些化合物的峰值电势比黄嘌呤高出400 mV以上。氧化过程中产生的UV吸附中间体的动力学还研究了中间产物在假一级反应中的衰变。对这两种化合物的氧化产物进行了分离和表征,并提出了初步的氧化机理。

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