Horikawa Manabu, Tateda Kazuhiro, Tuzuki Etsu, Ishii Yoshikazu, Ueda Chihiro, Takabatake Tohru, Miyairi Shinichi, Yamaguchi Keizou, Ishiguro Masaji
Suntory Institute for Bioorganic Research, Mishima-gun, Osaka 618-8503, Japan.
Bioorg Med Chem Lett. 2006 Apr 15;16(8):2130-3. doi: 10.1016/j.bmcl.2006.01.054. Epub 2006 Feb 7.
The synthesis of the analogs of N-3-oxododecanoyl-L-homoserine lactone (1) and their structure-activity relationship for the apoptotic induction in macrophages, P388D1 cells, are described. It was revealed that the position of the oxo group in the acyl side chain in addition to the presence of the L-homoserine lactone unit is crucial for the apoptosis-inducing activity. Furthermore, the long acyl side chains with hydrophobic distal ends are preferable for the activity.
描述了N-3-氧代十二烷酰-L-高丝氨酸内酯(1)类似物的合成及其对巨噬细胞P388D1细胞凋亡诱导的构效关系。结果表明,除了L-高丝氨酸内酯单元的存在外,酰基侧链中氧代基团的位置对凋亡诱导活性至关重要。此外,具有疏水末端的长酰基侧链对该活性更有利。