Department of Radiology, Washington University in St. Louis, 660 S. Euclid Avenue, St. Louis, Missouri 63110, United States.
Bioconjug Chem. 2011 Apr 20;22(4):752-8. doi: 10.1021/bc100550u. Epub 2011 Mar 24.
Norbuprenorphine-3-β-d-glucuronide (nBPN-3-β-d-G, 1) is a major phase II metabolite of buprenorphine, a pharmaceutical used for the treatment of opioid addiction. The pharmacological activity of compound 1 is not clear because investigations have been limited by the lack of chemically pure, well characterized 1 in sufficient quantities for in vitro and in vivo experiments. This work describes two concise, new methods of synthesis of 1, a chemical and an enzyme-assisted synthesis. The chemical synthesis used a strategy based on a combination of Koenig-Knorr coupling and amino-silyl protection. The enzyme-assisted synthesis used dog liver to convert the substrate norbuprenorphine (nBPN, 2) to 1. Both methods provided 1, characterized by (1)H NMR and tandem mass spectrometry, with purity >96%. The fractional yield of the enzyme-assisted synthesis was greater than that of the chemical synthesis (67% vs 5.3%), but due to larger reaction volumes, the chemical synthesis afforded greater amounts of total 1.
纳布啡-3-β-D-葡糖苷酸(nBPN-3-β-D-G,1)是丁丙诺啡的主要二期代谢物,丁丙诺啡是一种用于治疗阿片类药物成瘾的药物。由于缺乏化学纯、充分特征化的 1 用于体外和体内实验,因此对化合物 1 的药理学活性的研究受到限制。这项工作描述了两种简洁、新颖的 1 合成方法,一种是化学合成法,另一种是酶辅助合成法。化学合成采用基于 Koenig-Knorr 偶联和氨基硅烷基保护的策略。酶辅助合成使用狗肝将底物纳布啡(nBPN,2)转化为 1。这两种方法都提供了 1,通过(1)H NMR 和串联质谱进行了表征,纯度>96%。酶辅助合成的分数产率大于化学合成的分数产率(67%比 5.3%),但由于反应体积较大,化学合成提供了更多的总 1。