Inuki Shinsuke, Miyagawa Takashi, Oishi Shinya, Ohno Hiroaki
Graduate School of Pharmaceutical Sciences, Kyoto University.
Chem Pharm Bull (Tokyo). 2018;66(9):866-872. doi: 10.1248/cpb.c18-00366.
Sphingosine kinases (SphKs) are key enzymes that regulate sphingosine 1-phosphate production levels, and are involved in a range of cellular processes. Focusing on a hydrophilic residue in the hydrophobic binding pocket of SphKs, we designed and synthesized 4-epi-jaspine B derivatives containing a polar functional group in the lipid tail. A biological evaluation revealed that the introduction of ether groups to the lipid tail of 4-epi-jaspine B modulated its isoform selectivity toward SphKs.
鞘氨醇激酶(SphKs)是调节1-磷酸鞘氨醇生成水平的关键酶,参与一系列细胞过程。针对鞘氨醇激酶疏水结合口袋中的一个亲水残基,我们设计并合成了在脂尾中含有极性官能团的4-表茉莉刺桐碱B衍生物。生物学评价表明,在4-表茉莉刺桐碱B的脂尾引入醚基团可调节其对鞘氨醇激酶的亚型选择性。