Seoul National University Hospital, Seoul, Republic of Korea.
Department of Internal Medicine, Seoul National University College of Medicine, 101 Daehak-Ro, Chongno-gu, Seoul, 03080, Korea.
Drugs. 2016 Jul;76(10):1015-22. doi: 10.1007/s40265-016-0592-1.
Fimasartan is the ninth, and most recent, angiotensin II receptor antagonist approved as an antihypertensive agent. Fimasartan, a pyrimidin-4(3H)-one derivative of losartan with the imidazole ring replaced, which enables higher potency and longer duration than losartan. Fecal elimination and biliary excretion are the predominant elimination pathways of fimasartan and the urinary excretion was found to be less than 3 % 24 h after administration. Fimasartan is primarily catabolized by cytochrome P450 isoform 3A and no significant drug interaction was observed when used in combination with hydrochlorothiazide, amlodipine, warfarin, or digoxin. Fimasartan at a dosage range of 60-120 mg once daily showed an antihypertensive effect over 24 h. In a large, population-based observational study, fimasartan showed an excellent safety profile. Anti-inflammatory and organ-protecting effects of fimasartan have been shown in various preclinical studies, including aortic balloon injury, myocardial infarct ischemia/reperfusion, doxorubicin cardiotoxicity, and ischemic stroke models.
非马沙坦是第九个也是最新的血管紧张素 II 受体拮抗剂,被批准为抗高血压药物。非马沙坦是氯沙坦的嘧啶-4(3H)-酮衍生物,其中咪唑环被取代,使其比氯沙坦具有更高的效力和更长的作用持续时间。非马沙坦的主要消除途径是粪便排泄和胆汁排泄,给药后 24 小时内尿液排泄不到 3%。非马沙坦主要由细胞色素 P450 同工酶 3A 代谢,与氢氯噻嗪、氨氯地平、华法林或地高辛联合使用时未观察到明显的药物相互作用。非马沙坦的剂量范围为每天 60-120 毫克,一次,在 24 小时内显示出降压作用。在一项大型基于人群的观察性研究中,非马沙坦显示出良好的安全性。非马沙坦的抗炎和器官保护作用已在各种临床前研究中得到证实,包括主动脉球囊损伤、心肌梗死缺血/再灌注、多柔比星心脏毒性和缺血性中风模型。