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Synthesis solubility plasma stability and pharmacological evaluation of novel sulfonylhydrazones designed as anti-diabetic agents

机译:新型抗糖尿病药磺酰hydr的合成溶解度血浆稳定性和药理学评价

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摘要

Neuropathy is a serious complication of diabetes that has a significant socioeconomic impact, since it frequently demands high levels of health care consumption and compromises labor productivity. Recently, LASSBio-1471 (3) was demonstrated to improve oral glucose tolerance, reduce blood glucose levels, and display an anti-neuropathy effect in a murine streptozotocin-induced diabetes model. In the present work, we describe the design, synthesis, solubility, plasma stability, and pharmacological evaluation of novel sulfonylhydrazone derivatives (referred to herein as compounds 4–9), which were designed by molecular modification based on the structure of the prototype LASSBio-1471 (3). Among the compounds tested, better plasma stability was observed with 4, 5, and 9 in comparison to compounds 6, 7, and 8. LASSBio-1773 (7), promoted not only hypoglycemic activity but also the reduction of thermal hyperalgesia and mechanical allodynia in a murine model of streptozotocin-induced diabetic neuropathic pain.
机译:神经病是糖尿病的严重并发症,具有重大的社会经济影响,因为它经常需要高水平的医疗保健消费并损害劳动生产率。最近,在鼠链脲佐菌素诱导的糖尿病模型中,LASSBio-1471(3)被证明可改善口服葡萄糖耐量,降低血糖水平并显示出抗神经病作用。在本工作中,我们描述了新型磺酰hydr衍生物(在本文中称为化合物4-9)的设计,合成,溶解度,血浆稳定性和药理学评价,这些衍生物是根据原型LASSBio- 1471(3)。在测试的化合物中,与化合物6、7和8相比,使用4、5和9观察到更好的血浆稳定性。LASSBio-1773(7)不仅促进降血糖活性,而且还可以减少热痛觉过敏和机械性异常性疼痛。在链脲佐菌素诱导的糖尿病性神经性疼痛的小鼠模型中。

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