Department of Medicinal Chemistry, Merck Research Laboratories, P.O. Box 2000, Rahway, NJ 07065, USA.
Expert Opin Ther Pat. 2010 Sep;20(9):1219-45. doi: 10.1517/13543776.2010.510836.
Anemia caused by chronic kidney disease and other chronic diseases or conditions can be managed by the treatment of biologic-based erythropoiesis stimulating agents (ESAs). Although these ESAs are successful in treating these anemic conditions, a small molecule-based anti-anemia medicine can potentially revolutionize the treatment of anemia by bringing convenience to patients and being cost effective. Prolyl hydroxylase domain-containing protein (PHD) inhibitors may provide an opportunity for the development of small molecule anti-anemia medicines.
This review covers efforts to target PHD enzymes for stabilization of hypoxia-inducible factor (HIF)-alpha subunits under normal oxygen levels as an attractive strategy to upregulate the expression of erythropoietin and genes involved in iron metabolism for the treatment of anemia.
The reader will gain a brief summary of recent advances in HIF and PHD biology and a review of patents/patent applications on the subject of PHD inhibitors as HIF stabilizers for the treatment of anemia.
Several classes of PHD enzyme inhibitors have been disclosed and several are currently in clinical trials for the development of small molecule-based therapeutics for the treatment of anemia.
由慢性肾脏病和其他慢性疾病或病症引起的贫血,可以通过治疗基于生物的促红细胞生成刺激剂 (Esa) 来进行管理。虽然这些 Esa 在治疗这些贫血病症方面很成功,但小分子抗贫血药物有可能通过为患者带来便利并具有成本效益,从而彻底改变贫血的治疗方法。脯氨酰羟化酶结构域蛋白 (Phd) 抑制剂可能为开发小分子抗贫血药物提供机会。
本篇综述涵盖了靶向 Phd 酶以稳定低氧诱导因子 (Hif)-α亚基在正常氧水平下的努力,这是一种有吸引力的策略,可以上调促红细胞生成素和铁代谢相关基因的表达,从而治疗贫血。
读者将简要了解 Hif 和 Phd 生物学的最新进展,并对 Phd 抑制剂作为 Hif 稳定剂治疗贫血的专利/专利申请进行综述。
已经披露了几类 Phd 酶抑制剂,其中几种目前正在临床试验中,以开发用于治疗贫血的基于小分子的治疗药物。