Novak Rodger, Shlaes David M
Nabriva Therapeutics AG, Leberstrasse 20, 1110 Vienna, Austria.
Curr Opin Investig Drugs. 2010 Feb;11(2):182-91.
Pleuromutilins were discovered as natural-product antibiotics in 1950. Tiamulin was the first pleuromutilin compound to be approved for veterinary use in 1979, followed by valnemulin in 1999. It was not until 2007 that retapamulin became the first pleuromutilin approved for use in humans. However, retapamulin is limited to topical application. Recent advances in lead optimization have led to the synthesis of pleuromutilins that combine potent antibacterial activity with favorable pharmaceutical properties, making these compounds suitable for oral and intravenous delivery. Most pleuromutilins have an antibacterial spectrum that spans the common pathogens involved in both skin and respiratory tract infections. Two new pleuromutilins, BC-3205 and BC-7013 (both Nabriva Therapeutics AG), have entered clinical trials. In this review, the key properties of pleuromutilin derivatives, designed primarily through modifications at the C(14) side chain, are presented, and the potential of these compounds in systemic therapy in humans is discussed.
截短侧耳素类抗生素于1950年作为天然产物抗生素被发现。替米考星是1979年首个被批准用于兽医领域的截短侧耳素类化合物,随后1999年批准了沃尼妙林。直到2007年,瑞他帕林才成为首个被批准用于人类的截短侧耳素类药物。然而,瑞他帕林仅限于局部应用。先导化合物优化方面的最新进展已导致合成出兼具强效抗菌活性和良好药学性质的截短侧耳素类化合物,使这些化合物适合口服和静脉给药。大多数截短侧耳素类抗生素的抗菌谱涵盖皮肤和呼吸道感染中常见的病原体。两种新型截短侧耳素类药物BC - 3205和BC - 7013(均来自纳布瑞瓦治疗公司)已进入临床试验阶段。在本综述中,主要介绍了主要通过对C(14)侧链进行修饰设计的截短侧耳素类衍生物的关键特性,并讨论了这些化合物在人类全身治疗中的潜力。