Microbial synthesis of a deuterium-labelled metabolite of an NK1 receptor antagonist, TAK-637
作者:Naoki Tarui、Yoshinori Ikeura、Hideaki Natsugari、Kazuo Nakahama
DOI:10.1002/jlcr.513
日期:2001.10.30
Microbial conversion of deuterium-labelled TAK-637 ((aR,9S)-[10,10,11, 11-2H4]-7-[3,5-bis(trifluoromethyl)benzyl]-8,9,10,11-tetrahydro-9-methyl-5-(4-methylphenyl)-7H-[1,4]diazocino[2,1-g][1,7]naphthyridine-6,13-dione, 1) was carried out using Streptomyces subrutilus IFO13388 to give a deuterium-labelled hydroxylated TAK-637 ((aR,9S)- [10,10,11,11-2H4]-7-[3,5-bis(trifluoromethyl)benzyl]-8,9,10,11-tetrahydro-9-methyl-5-(4-hydroxymethylphenyl)-7H-[1,4]diazocino[2,1-g][1,7]naphthyridine-6,13-dione, 2) for use as an internal standard in LC-MS studies. Copyright © 2001 John Wiley & Sons, Ltd.
氘标记 TAK-637 ((aR,9S)-[10,10,11, 11-2H4]-7-[3,5-双(三氟甲基)苄基]-8,9,10,11- 的微生物转化四氢-9-甲基-5-(4-甲基苯基)-7H-[1,4]重氮杂环[2,1-g][1,7]萘啶-6,13-二酮, 1) 使用Streptomyces subrutilus进行IFO13388 得到氘标记的羟基化 TAK-637 ((aR,9S)- [10,10,11,11-2H4]-7-[3,5-双(三氟甲基)苄基]-8,9,10, 11-四氢-9-甲基-5-(4-羟甲基苯基)-7H-[1,4]重氮杂环[2,1-g][1,7]萘啶-6,13-二酮,2)用作LC-MS 研究中的内标。版权所有 © 2001 约翰·威利父子有限公司