化学
立体中心
手性(物理)
对映体
药品
立体化学
组合化学
药理学
对映选择合成
生物化学
物理
催化作用
量子力学
夸克
Nambu–Jona Lasinio模型
手征对称破缺
医学
作者
Rebecca McVicker,Niamh M. O’Boyle
标识
DOI:10.1021/acs.jmedchem.3c02239
摘要
Many drugs are chiral with their chirality determining their biological interactions, safety, and efficacy. Since the 1980s, there has been a regulatory preference to bring single enantiomer to market. This perspective discusses trends related to chirality that have developed in the past decade (2013-2022) of new drug approvals. The EMA has not approved a racemate since 2016, while the average for the FDA is one per year from 2013 to 2022. These 10 include drugs which have been previously marketed elsewhere for several decades, analogues of pre-existing drugs, or drugs where the undefined stereocenter does not play a role in therapeutic activity. Two chiral switches were identified which were both combined with drug repurposing. This combination strategy has the potential to produce therapeutically valuable drugs in a faster time frame. Two class III atropisomers displaying axial chirality were approved between 2013 and 2022, one as a racemate and one as a single enantiomer.
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