Simić Stefan, Zukić Erna, Schmermund Luca, Faber Kurt, Winkler Christoph K, Kroutil Wolfgang
Institute of Chemistry, University of Graz, NAWI Graz, Heinrichstraße 28, 8010 Graz, Austria.
Field of Excellence BioHealth─University of Graz, 8010 Graz, Austria.
Chem Rev. 2022 Jan 12;122(1):1052-1126. doi: 10.1021/acs.chemrev.1c00574. Epub 2021 Nov 30.
Biocatalysis, using enzymes for organic synthesis, has emerged as powerful tool for the synthesis of active pharmaceutical ingredients (APIs). The first industrial biocatalytic processes launched in the first half of the last century exploited whole-cell microorganisms where the specific enzyme at work was not known. In the meantime, novel molecular biology methods, such as efficient gene sequencing and synthesis, triggered breakthroughs in directed evolution for the rapid development of process-stable enzymes with broad substrate scope and good selectivities tailored for specific substrates. To date, enzymes are employed to enable shorter, more efficient, and more sustainable alternative routes toward (established) small molecule APIs, and are additionally used to perform standard reactions in API synthesis more efficiently. Herein, large-scale synthetic routes containing biocatalytic key steps toward >130 APIs of approved drugs and drug candidates are compared with the corresponding chemical protocols (if available) regarding the steps, reaction conditions, and scale. The review is structured according to the functional group formed in the reaction.
生物催化,即利用酶进行有机合成,已成为合成活性药物成分(API)的有力工具。上世纪上半叶推出的首批工业生物催化工艺利用的是全细胞微生物,当时起作用的特定酶并不明确。与此同时,新型分子生物学方法,如高效基因测序和合成,引发了定向进化的突破,从而能够快速开发出具有广泛底物范围且针对特定底物量身定制的良好选择性的工艺稳定型酶。迄今为止,酶被用于实现通往(已有的)小分子API的更短、更高效和更可持续的替代路线,并且还被用于更高效地进行API合成中的标准反应。在此,将包含生物催化关键步骤通往130多种已批准药物和候选药物API的大规模合成路线与相应的化学方案(若有)在步骤、反应条件和规模方面进行比较。本综述根据反应中形成的官能团进行编排。