Shi Sophia M, Di Li
a Cornell University , Ithaca , NY , USA.
b Pfizer Inc ., Groton , CT , USA.
Expert Opin Drug Metab Toxicol. 2017 Aug;13(8):859-870. doi: 10.1080/17425255.2017.1356820.
Carbonyl reductase 1 (CBR1) plays a critical role in drug metabolism of ketones and aldehydes. CBR1 has broad substrate specificity and is involved in metabolizing a number of clinically important drugs. Areas covered: The impact of CBR1 in drug metabolism and disposition are discussed. The CBR1 enzyme is covered in detail including discussion on topics such as tissue distribution, species difference, individual variability, the effect of genetic polymorphism and disease state, iGnducibility and drug-drug interaction potential. The structure and function of CBR1 and CBR3 are also compared. In addition, the formation of chiral alcohols from CBR1 reduction and MIST coverage are reviewed. Expert Opinion: As CBR1 is an emerging enzyme in drug discovery and development, much research is needed to further understand its role in drug metabolism and disposition. In vitro-in vivo correlation for CBR1-mediated clearance is mostly unknown. Selective CBR1 inhibitors and substrates are not well enough characterized for reaction phenotyping of the CBR1 pathway. Multiple pathways appear to be involved in the regulation of CBR1. Future investigation will also help reveal their impact on drug-drug interaction potentials and the influence of individual variability.
羰基还原酶1(CBR1)在酮类和醛类药物代谢中起关键作用。CBR1具有广泛的底物特异性,参与多种临床重要药物的代谢。涵盖领域:讨论了CBR1在药物代谢和处置中的影响。详细介绍了CBR1酶,包括组织分布、物种差异、个体变异性、基因多态性和疾病状态的影响、诱导性以及药物相互作用潜力等主题。还比较了CBR1和CBR3的结构与功能。此外,综述了CBR1还原生成手性醇的过程以及MIST覆盖情况。专家观点:由于CBR1是药物研发中一种新出现的酶,需要开展大量研究以进一步了解其在药物代谢和处置中的作用。CBR1介导的清除率的体外-体内相关性大多未知。用于CBR1途径反应表型分析的选择性CBR1抑制剂和底物的特性尚不充分。似乎有多种途径参与CBR1的调节。未来的研究也将有助于揭示它们对药物相互作用潜力的影响以及个体变异性的影响。