Boss Christoph, Bolli Martin H, Gatfield John
Drug Discovery and Preclinical Research, Actelion Pharmaceuticals Ltd, Gewerbestrasse 16, CH-4123 Allschwil/BL, Switzerland.
Drug Discovery and Preclinical Research, Actelion Pharmaceuticals Ltd, Gewerbestrasse 16, CH-4123 Allschwil/BL, Switzerland.
Bioorg Med Chem Lett. 2016 Aug 1;26(15):3381-94. doi: 10.1016/j.bmcl.2016.06.014. Epub 2016 Jun 10.
The endothelin peptides bind to two receptors found on cells of vasculature and in tissues. While the endothelin-A (ETA)-receptor is predominantly expressed in vascular smooth muscle cells, the endothelin-B (ETB)-receptor is also found in endothelial cells, fibroblasts, and neuronal cells. Activation of the endothelin system plays a driving role in several chronic cardiovascular diseases and several endothelin receptor antagonists (ERAs) (bosentan (6), ambrisentan (83) and macitentan (43)) have successfully been introduced as oral treatments for the life threatening condition of pulmonary arterial hypertension (PAH). This digest highlights the medicinal chemistry of the pyrimidine based ERAs 6 and 43 and describes the story that started with bosentan and culminated in macitentan (43). A condensed overview of the competitive landscape in the field of ERAs puts the different strategies and tactics applied by the medicinal chemists involved in this endeavor into perspective.
内皮素肽可与血管系统细胞和组织中的两种受体结合。内皮素A(ETA)受体主要在血管平滑肌细胞中表达,而内皮素B(ETB)受体也存在于内皮细胞、成纤维细胞和神经细胞中。内皮素系统的激活在几种慢性心血管疾病中起驱动作用,几种内皮素受体拮抗剂(ERA)(波生坦(6)、安立生坦(83)和马昔腾坦(43))已成功作为口服药物用于治疗危及生命的肺动脉高压(PAH)。本综述重点介绍了基于嘧啶的ERA 6和43的药物化学,并描述了从波生坦开始并最终研发出马昔腾坦(43)的历程。对ERA领域竞争格局的简要概述,使参与这一努力的药物化学家所采用的不同策略和战术一目了然。