Synthesis and evaluation of acyl protein thioesterase 1 (APT1) inhibitors

被引:36
作者
Biel, Markus
Deck, Patrick
Giannis, Athanassios
Waldmann, Herbert
机构
[1] Univ Liepzig, Inst Organ Chem, D-04103 Leipzig, Germany
[2] Max Planck Inst Mol Physiol, Dept Chem Biol, D-44227 Dortmund, Germany
[3] Univ Dortmund, Dept Chem Biol, D-44227 Dortmund, Germany
关键词
palmitoylation; peptidomimetics; proteins; signal transduction;
D O I
10.1002/chem.200501128
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lipid-modified proteins play decisive roles in important biological processes such as signal transduction, organisation of the cytoskeleton and vesicular transport. Lipidation of these proteins is essential for correct biological function. Among the modifications with lipids, prenylation and myristoylation are well understood. However, the machinery of palmitoylation is still under investigation. Recently, an enzyme, acyl protein thioesterase 1 (APTI), that may play a regulatory role in the palmitoylation cycle of H-Ras and G-protein a subunits, was purified. Motivated by this work, several inhibitors of APT1 were designed, synithesized and biologically evaluated leading to highly active compounds.
引用
收藏
页码:4121 / 4143
页数:23
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