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首页> 外文期刊>ChemMedChem >Discovery of Molidustat (BAY85-3934): A Small-Molecule Oral HIF-Prolyl Hydroxylase (HIF-PH) Inhibitor for the Treatment of Renal Anemia
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Discovery of Molidustat (BAY85-3934): A Small-Molecule Oral HIF-Prolyl Hydroxylase (HIF-PH) Inhibitor for the Treatment of Renal Anemia

机译:Molidustat(Bay85-3934)的发现:用于治疗肾贫血的小分子口腔HIF-脯氨酰羟化酶(HIF-pH)抑制剂

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Small-molecule inhibitors of hypoxia-inducible factor prolyl hydroxylases (HIF-PHs) are currently under clinical development as novel treatment options for chronic kidney disease (CKD) associated anemia. Inhibition of HIF-PH mimics hypoxia and leads to increased erythropoietin (EPO) expression and subsequently increased erythropoiesis. Herein we describe the discovery, synthesis, structure-activity relationship (SAR), and proposed binding mode of novel 2,4-diheteroaryl-1,2-dihydro-3H-pyrazol-3-ones as orally bioavailable HIF-PH inhibitors for the treatment of anemia. High-throughput screening of our corporate compound library identified BAY-908 as a promising hit. The lead optimization program then resulted in the identification of molidustat (BAY85-3934), a novel small-molecule oral HIF-PH inhibitor. Molidustat is currently being investigated in clinical phaseIII trials as molidustat sodium for the treatment of anemia in patients with CKD.
机译:缺氧诱导因子脯氨酰酶(HIF-pH)的小分子抑制剂目前正在临床开发中作为慢性肾病(CKD)相关贫血的新型治疗方案。 抑制HIF-pH模拟缺氧,并导致促红细胞生成素(EPO)表达增加,随后增加促红细胞生成。 在此,我们描述了新型2,4-二烷基-1,2-二氢-3H-吡唑-3-作为口服生物可利用的HIF-pH抑制剂的新型2,4-二烷基-1,2-二氢-3-Pyrozol-3-的发现,合成,结构 - 活性关系(SAR)和提出的结合模式 治疗贫血。 我们公司复合图书馆的高吞吐量筛选确定了Bay-908作为有希望的击中。 然后导致铅优化程序导致Molidustat(Bay85-3934),一种新型小分子口腔HIF-pH抑制剂。 目前正在研究Molidustat作为Molidustat钠的临床研究,用于治疗CKD患者贫血。

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