Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto 862-0973, Japan.
Bioorg Med Chem Lett. 2010 Jun 1;20(11):3341-3. doi: 10.1016/j.bmcl.2010.04.029. Epub 2010 Apr 14.
Aaptamine (1), isoaaptamine (2), and demethylaaptamine (3) were isolated from the marine sponge Aaptossuberitoides collected in Indonesia as inhibitors of the proteasome. They inhibited the chymotrypsin-like and caspase-like activities of the proteasome with IC(50) values of 1.6-4.6 microg/mL, while they showed less inhibition of the trypsin-like activity of the proteasome. The three compounds showed cytotoxic activities against HeLa cells, but their cytotoxicity did not correlate with their potency as proteasome inhibitors, strongly suggesting that their proteasomal inhibitory activity is dispensable to their cytotoxicity.
阿朴菲定(1)、异阿朴菲定(2)和去甲基阿朴菲定(3)是从印度尼西亚采集的海绵 Aaptossuberitoides 中分离得到的蛋白酶体抑制剂。它们对蛋白酶体的糜蛋白酶样和半胱天冬酶样活性的抑制 IC50 值为 1.6-4.6μg/mL,而对蛋白酶体的胰蛋白酶样活性的抑制作用较弱。这三种化合物对 HeLa 细胞均表现出细胞毒性,但它们的细胞毒性与其作为蛋白酶体抑制剂的效力没有相关性,这强烈表明它们的蛋白酶体抑制活性对其细胞毒性不是必需的。