Deep understanding of the interaction between thienorphine and UDP-glucuronosyltransferase (UGT) isoforms

Deep understanding of the interaction between thienorphine and UDP-glucuronosyltransferase (UGT) isoforms
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深入了解噻诺啡和 UDP-葡萄糖醛酸基转移酶 (UGT) 亚型之间的相互作用

DOI:
10.3109/00498254.2012.706723
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发表时间:
2013-01
期刊:
影响因子:
1.8
通讯作者:
Yang, Ling
Yang, Ling
中科院分区:
医学4区
文献类型:
--
作者:
Liu, Ze-Yuan;Fang, Zhong-Ze;Zhu, Liang-Liang;Ge, Guang-Bo;Li, Xiao-Bao;Hu, Cui-Min;Cao, Yun-Feng;Xia, Yang-Liu;Yang, Ling

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噻吩诺啡已被证明是一种强效、长效的部分阿片类激动剂。它正在被开发为治疗阿片类药物依赖的良好候选药物。噻吩诺啡与人肝微粒体孵育后,检测到噻吩诺啡的葡萄糖醛酸苷。
Thienorphine has been demonstrated to be a potent, long-acting partial opioid agonist. It is being developed as a good candidate to treat opioid dependence. The thienorphine’s glucuronide was detected after thienorphine was incubated with human liver micr
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