Zhang Initiative Research Unit, Institute Laboratories, RIKEN, Wako, Saitama, Japan.
Bioorg Med Chem Lett. 2013 Sep 15;23(18):5145-9. doi: 10.1016/j.bmcl.2013.07.022. Epub 2013 Jul 19.
SUMO activating enzyme 1 (SUMO E1) is the first enzyme in sumoylation pathway and an important cancer drug target. However, only a few inhibitors were reported up to now that includes three natural products, semi-synthetic protein inhibitors and one AMP mimic. Here, we report the identification of quinazolinyloxy biaryl urea as a new class of SUMO E1 inhibitors. The most active compound of this class inhibited the in vitro sumoylation with an IC50 of 13.4 μM. This compound inhibits sumoylation by blocking the formation of SUMOE1-SUMO thioester intermediate. The biological activity of the most active compound is comparable to previously reported inhibitors with properties suitable for medicinal chemistry optimization for potency and druggability.
SUMO 激活酶 1(SUMO E1)是 sumoylation 途径中的第一种酶,也是一个重要的癌症药物靶点。然而,到目前为止,仅报道了少数几种抑制剂,包括三种天然产物、半合成蛋白抑制剂和一种 AMP 类似物。在这里,我们报道了喹唑啉氧基联苯脲作为一种新型 SUMO E1 抑制剂的鉴定。该类中最活跃的化合物对体外 sumoylation 的抑制 IC50 为 13.4 μM。该化合物通过阻止 SUMOE1-SUMO 硫酯中间体的形成来抑制 sumoylation。最活跃化合物的生物学活性可与先前报道的抑制剂相媲美,具有适合药物化学优化的效力和可药性。