Discovery of Molidustat (BAY85-3934): A Small-Molecule Oral HIF-Prolyl Hydroxylase (HIF-PH) Inhibitor for the Treatment of Renal Anemia

被引:55
|
作者
Beck, Hartmut [1 ]
Jeske, Mario [1 ]
Thede, Kai [2 ]
Stoll, Friederike [1 ]
Flamme, Ingo [3 ]
Akbaba, Metin [1 ]
Ergueden, Jens-Kerim [1 ]
Karig, Gunter [1 ]
Keldenich, Joerg [4 ]
Oehme, Felix [3 ]
Militzer, Hans-Christian [5 ]
Hartung, Ingo V. [2 ]
Thuss, Uwe [4 ]
机构
[1] Bayer AG, Med Chem Wuppertal, D-42096 Wuppertal, Germany
[2] Bayer AG, Med Chem Berlin, D-13342 Berlin, Germany
[3] Bayer AG, Cardiol Res Wuppertal, D-42096 Wuppertal, Germany
[4] Bayer AG, DMPK Wuppertal, D-42096 Wuppertal, Germany
[5] Bayer AG, Chem Dev Wuppertal, D-42096 Wuppertal, Germany
关键词
BAY85-3934; HIF-PH; inhibitors; metalloenzymes; molidustat; HYPOXIA-INDUCIBLE FACTOR; WHOLE-CELL BIOTRANSFORMATION; CHRONIC KIDNEY-DISEASE; METABOLITES; FAMILY;
D O I
10.1002/cmdc.201700783
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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.
引用
收藏
页码:988 / 1003
页数:16
相关论文
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