Cone E J, Gorodetzky C W, Yeh S Y
J Pharm Sci. 1975 Apr;64(4):618-21. doi: 10.1002/jps.2600640409.
Chemical reduction of naltrexone is described in an attempt to synthesize 6-beta-hydroxynaltrexone. Only the epimer, 6-alpha-hydroxynaltrexone, was produced. Pilot metabolic studies on naltrexone in the dog, rat, and guinea pig were made to determine which animal produced the greatest amount of 6-beta-hydroxynaltrexone. The guinea pig was selected and used to produce the metabolite. Isolation and purification methods are described, and spectral data are presented for structural confirmation of the metabolite.
为了合成6-β-羟基纳曲酮,对纳曲酮进行了化学还原。结果只生成了差向异构体6-α-羟基纳曲酮。对狗、大鼠和豚鼠进行了纳曲酮的初步代谢研究,以确定哪种动物产生的6-β-羟基纳曲酮量最大。选择豚鼠来生成这种代谢物。描述了分离和纯化方法,并给出了光谱数据以对代谢物进行结构确证。