Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Strasse 11, 44227 Dortmund, Germany.
Chembiochem. 2013 Jan 2;14(1):115-22. doi: 10.1002/cbic.201200571. Epub 2012 Dec 13.
Ras proteins are of importance in cell proliferation, and hence their mutated forms play causative roles in many kinds of cancer in different tissues. Inhibition of the Ras-depalmitoylating enzyme acyl protein thioesterases APT1 and -2 is a new approach to modulating the Ras cycle. Here we present boronic and borinic acid derivatives as a new class of potent and nontoxic APT inhibitors. These compounds were detected by extensive library screening using chemical arrays and turned out to inhibit human APT1 and -2 in a competitive mode. Furthermore, one of the molecules was demonstrated to inhibit Erk1/2 phosphorylation significantly.
Ras 蛋白在细胞增殖中具有重要作用,因此其突变形式在不同组织的多种癌症中起致病作用。抑制 Ras 去棕榈酰化酶酰基蛋白硫酯酶 APT1 和 -2 是调节 Ras 循环的新方法。在这里,我们提出了硼酸和硼酸衍生物作为一类新的强效和无毒的 APT 抑制剂。这些化合物通过使用化学阵列的广泛文库筛选被检测到,并被证明以竞争性模式抑制人 APT1 和 -2。此外,其中一种分子被证明可显著抑制 Erk1/2 磷酸化。