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Selective thyroid hormone receptor β agonists with oxadiazolone acid isosteres.
Bioorganic & Medicinal Chemistry Letters ( IF 2.7 ) Pub Date : 2020-08-05 , DOI: 10.1016/j.bmcl.2020.127465
Thorsten A Kirschberg 1 , Christopher T Jones 1 , Yingzi Xu 1 , Martijn Fenaux 1 , Randall L Halcomb 1 , Yujin Wang 1 , Kevin Klucher 1
Affiliation  

Use of the oxadiazolone acid isostere in triiodothyronine analogs yielded potent and selective agonists for the thyroid hormone receptor β. Selected examples showed good in-vivo efficacy in a rat hypercholesterolemic model. One compound was further profiled in a diet-induced mouse model of nonalcoholic steatohepatitis (NASH) and showed robust target engagement and significant histological improvements in both liver steatosis and fibrosis.



中文翻译:

与恶二唑酮酸等排物的选择性甲状腺激素受体β激动剂。

在三碘甲腺嘌呤类似物中使用恶二唑酮酸等排酮可产生有效且选择性的甲状腺激素受体β激动剂。选定的实例在大鼠高胆固醇血症模型中显示出良好的体内功效。在饮食诱导的非酒精性脂肪性肝炎(NASH)小鼠模型中进一步分析了一种化合物,该化合物在肝脂肪变性和纤维化中均显示出强大的靶标参与性和明显的组织学改善。

更新日期:2020-08-29
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