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Synthesis and Liver Microsomal Metabolic Stability Studies of a Fluorine-Substituted δ-Tocotrienol Derivative.
ChemMedChem ( IF 3.4 ) Pub Date : 2020-01-19 , DOI: 10.1002/cmdc.201900676
Xingui Liu 1, 2 , Saikat Poddar 3 , Lin Song 1 , Howard Hendrickson 1, 4 , Xuan Zhang 1, 3 , Yaxia Yuan 2 , Daohong Zhou 1, 2 , Guangrong Zheng 1, 3
Affiliation  

A fluoro-substituted δ-tocotrienol derivative, DT3-F2, was synthesized. This compound was designed to stabilize the metabolically labile terminal methyl groups of δ-tocotrienol by replacing one C-H bond on each of the two methyl groups with a C-F bond. However, in vitro metabolic stability studies using mouse liver microsomes revealed an unexpected rapid enzymatic C-F bond hydrolysis of DT3-F2. To the best of our knowledge, this is the first report of an unusual metabolic hydrolysis of allylic C-F bonds.

中文翻译:

氟代δ-生育三烯酚衍生物的合成及其肝微粒体代谢稳定性研究。

合成了氟取代的δ-生育三烯酚衍生物DT3-F2。该化合物被设计为通过用CF键取代两个甲基上每个的一个CH键来稳定δ-生育三烯酚的代谢不稳定的甲基。但是,使用小鼠肝微粒体进行的体外代谢稳定性研究表明,DT3-F2发生了意外的快速酶促CF键水解。据我们所知,这是烯丙基CF键异常代谢水解的第一个报道。
更新日期:2020-02-11
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