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Structure-Activity Relationship and Crystallographic Studies on 4-Hydroxypyrimidine HIF Prolyl Hydroxylase Domain Inhibitors.
ChemMedChem ( IF 3.4 ) Pub Date : 2019-11-21 , DOI: 10.1002/cmdc.201900557
James P Holt-Martyn 1 , Rasheduzzaman Chowdhury 1 , Anthony Tumber 1 , Tzu-Lan Yeh 1 , Martine I Abboud 1 , Kerstin Lippl 1 , Christopher T Lohans 1 , Gareth W Langley 1 , William Figg 1 , Michael A McDonough 1 , Christopher W Pugh 2 , Peter J Ratcliffe 2, 3 , Christopher J Schofield 1
Affiliation  

The 2-oxoglutarate-dependent hypoxia inducible factor prolyl hydroxylases (PHDs) are targets for treatment of a variety of diseases including anaemia. One PHD inhibitor is approved for use for the treatment of renal anaemia and others are in late stage clinical trials. The number of reported templates for PHD inhibition is limited. We report structure-activity relationship and crystallographic studies on a promising class of 4-hydroxypyrimidine-containing PHD inhibitors.

中文翻译:

4-羟基嘧啶 HIF 脯氨酰羟化酶结构域抑制剂的构效关系和晶体学研究。

2-酮戊二酸依赖性缺氧诱导因子脯氨酰羟化酶 (PHD) 是治疗包括贫血在内的多种疾病的靶标。一种 PHD 抑制剂被批准用于治疗肾性贫血,其他抑制剂正处于后期临床试验中。已报道的 PHD 抑制模板数量有限。我们报告了一类有前途的含 4-羟基嘧啶的 PHD 抑制剂的构效关系和晶体学研究。
更新日期:2019-12-03
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