药品
药理学
肝损伤
克
化学
医学
生物
细菌
遗传学
作者
Bo Ma,Zhenwei Wang,Xiaoyu Liu,M Wang,Yongwang Zhang,Meng Zhang,Xiaozhen Jiao,Ping Xie
标识
DOI:10.1080/10286020.2023.2270440
摘要
Bicyclol, an innovative hepatoprotective drug, was approved by the Chinese National Medical Products Administration (NMPA) in 2001 to treat Hepatitis B and drug-induced liver injury. Two active metabolites of bicyclol have been identified as M2 and M3. To evaluate the impact on drug safety and efficacy of possible drug-drug interactions (DDIs) associated with these metabolites, a sufficient quantity of these metabolites is required. Herein, we report a concise novel route for the synthesis of M2 and M3 using the Suzuki-Miyaura coupling as the key step. Furthermore, we complete the gram-scale syntheses of M2 and M3.
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