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首页> 外文期刊>The Journal of Organic Chemistry >Chasing the Elusive Benzofuran Impurity of the THR Antagonist NH-3: Synthesis, Isotope Labeling, and Biological Activity
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Chasing the Elusive Benzofuran Impurity of the THR Antagonist NH-3: Synthesis, Isotope Labeling, and Biological Activity

机译:追逐THR拮抗剂NH-3的难以捉摸的苯并呋喃杂质:合成,同位素标记和生物活性

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摘要

We have synthesized and established the structure of a long-suspected, but hitherto unknown, benzofuran side product (EBI) formed during the synthesis of NH-3. Understanding the mechanism of its formation has enabled isotope (D) labeling. We further developed a highly efficient method for separating EBI from NH-3. Interestingly, EBI was found to be a very potent thyroid hormone receptor (THR) agonist, while NH-3 is an antagonist. In this process, we have also achieved a significantly improved synthesis of NH-3.
机译:我们已经合成并建立了在NH-3合成过程中形成的,长期以来仍被怀疑但迄今未知的苯并呋喃副产物(EBI)的结构。了解其形成机理已实现了同位素(D)标记。我们进一步开发了一种从NH-3中分离EBI的高效方法。有趣的是,发现EBI是非常有效的甲状腺激素受体(THR)激动剂,而NH-3是拮抗​​剂。在这一过程中,我们还实现了NH-3合成的显着改善。

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