Kim Ho Shin, Hammill Jared T, Guy R Kiplin
Department of Pharmaceutical Sciences, University of Kentucky , Lexington, Kentucky 40508, United States.
J Med Chem. 2017 Apr 13;60(7):2651-2653. doi: 10.1021/acs.jmedchem.7b00299. Epub 2017 Mar 15.
The majority of frontline therapies for the treatment of malaria are combination drugs containing artemisinin (or its semisynthetic analogs), known as artemisinin combination therapies (ACTs). While generally efficacious, ACTs and the first generation fully synthetic ozonide, arterolane (OZ277, 1), suffer from rapid clearance requiring 3-day dosing regimens. Extensive structure-activity studies led to the discovery of a second-generation ozonide, artefenomel (OZ439, 2), which has overcome this limitation, maintaining the rapid onset of action and potent activity of the artemisinin derivatives while exhibiting greatly improved pharmacokinetics, low projected cost of goods, prophylactic activity, and the potential for a single dose cure.
治疗疟疾的大多数一线疗法是含有青蒿素(或其半合成类似物)的复方药物,即青蒿素联合疗法(ACTs)。虽然ACTs和第一代全合成臭氧化物蒿甲醚(OZ277,1)通常有效,但它们存在清除速度快的问题,需要3天的给药方案。广泛的构效关系研究导致发现了第二代臭氧化物,即青蒿甲醚(OZ439,2),它克服了这一局限性,在保持青蒿素衍生物快速起效和强效活性的同时,展现出大大改善的药代动力学、较低的预计生产成本、预防活性以及单剂量治愈的潜力。