Department of Chemistry - BMC, Uppsala University, Box 576, SE-751 23 Uppsala, Sweden.
Department of Medicinal Chemistry, MIPS, Monash University, 381 Royal Parade, Parkville, Victoria, Australia.
Curr Opin Chem Biol. 2018 Jun;44:23-29. doi: 10.1016/j.cbpa.2018.05.010. Epub 2018 May 25.
Recent years have seen a dramatic increase in the number of drugs approved in chemical space outside of Lipinski's rule of 5, that is in what has been termed beyond rule of 5 (bRo5) space. The development of three major classes of oral drugs that treat HIV and HCV infections and the growing evidence that novel, difficult targets can be accessed has prompted research into understanding design of drugs displaying cell permeability, solubility and ultimately oral bioavailability in bRo5 space. Studies have found a consistent outer property limit for a reasonable chance of de novo designing oral bioavailability. In addition, several property-based guidelines, along with incorporation of chameleonic features, have emerged as strategies to aid design in bRo5 space. A more detailed understanding of the complex and environment dependent conformational landscape will likely be the focus of the next generation of guidelines allowing property predictions of ever more complex compounds. By pushing the boundaries of current orally designable chemical space we hope that discoveries will be made for fundamental science and also for discovery of novel therapeutics.
近年来,在 Lipinski 五规则之外的化学空间中批准的药物数量急剧增加,也就是说,在所谓的超出五规则(bRo5)空间中。治疗 HIV 和 HCV 感染的三类主要口服药物的发展以及越来越多的证据表明,新型、难以攻克的靶点可以被触及,这促使人们研究理解在 bRo5 空间中显示细胞通透性、溶解度和最终口服生物利用度的药物设计。研究发现,对于合理设计口服生物利用度,存在一个一致的外部属性限制。此外,随着一些基于属性的指南的出现,以及变色龙特征的融入,已经出现了一些策略来帮助 bRo5 空间中的设计。更详细地了解复杂且依赖环境的构象景观,可能是下一代指南的重点,这些指南将允许对越来越复杂的化合物进行属性预测。通过推动当前口服可设计化学空间的界限,我们希望能够为基础科学和新型治疗药物的发现做出贡献。