首页> 外文期刊>Journal of the Chemical Society, Perkin Transactions 1 >Novel xanthine oxidase inhibitor studies. Part 2. Synthesis and xanthine oxidase inhibitory activities of 2-substituted 6-alkyl-idenehydrazino- or 6-arylmethylidenehydrazino-7H-purines and 3- and/or 5-substituted 9H-1, 2, 4-triazolo[3, 4-i]purines
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Novel xanthine oxidase inhibitor studies. Part 2. Synthesis and xanthine oxidase inhibitory activities of 2-substituted 6-alkyl-idenehydrazino- or 6-arylmethylidenehydrazino-7H-purines and 3- and/or 5-substituted 9H-1, 2, 4-triazolo[3, 4-i]purines

机译:新的黄嘌呤氧化酶抑制剂研究。第2部分。2-取代的6-烷基亚烷基肼基-或6-芳基亚甲基肼基-7H-嘌呤和3-和/或5-取代的9H-1、2、4-三唑并[3,4-的合成和黄嘌呤氧化酶抑制活性我]嘌呤

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摘要

The facile and general synthesis of 2-substituted 6-alkylidenehydrazino- or 6-arylmethylidenehydrazino-7H-purines and 3- and/or 5-substituted 9H-1, 2, 4-triazolo[3, 4-i]purines, which were obtained by oxidative cyclisation of the corresponding 6-aldehyde hydrazones of 7H-purine, as a new class of potential xanthine oxidase inhibitors are reported. Their inhibitory activities against bovine milk xanthine oxidase in vitro were also investigated, and some purines 2 and 6 and triazolopurines 7 exhibited from several times to several hundred times more potent activities than allopurinol.
机译:2取代的6-亚烷基萘并肼或6-芳基亚甲基肼并-7H-嘌呤和3-和/或5-取代的9H-1,2,4-三唑并[3,4-i]嘌呤的简便且通用的合成方法通过对7H-嘌呤的相应的6-醛azo酮进行氧化环化获得的新型潜在的黄嘌呤氧化酶抑制剂已有报道。还研究了它们在体外对牛黄嘌呤氧化酶的抑制活性,一些嘌呤2和6和三唑并呋喃酮7的活性比别嘌呤醇高出几倍到几百倍。

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