Jang Kyoung Hwa, Chung Soon-Chun, Shin Jongheon, Lee So-Hyoung, Kim Tae-Im, Lee Hyi-Seung, Oh Ki-Bong
Natural Products Research Institute, College of Pharmacy, Seoul National University, Seoul 110-460, Republic of Korea.
Bioorg Med Chem Lett. 2007 Oct 1;17(19):5366-9. doi: 10.1016/j.bmcl.2007.08.007. Epub 2007 Aug 11.
Four aaptamines (1-4), 1H-benzo[de][1,6]-naphthyridine alkaloids, were isolated from the marine sponge Aaptos aaptos and their inhibitory activities against sortase A (SrtA), an enzyme that plays a key role in cell wall protein anchoring and virulence in Staphylococcus aureus, were evaluated. Isoaaptamine (2) was a potent inhibitor of SrtA, with an IC(50) value of 3.7+/-0.2 microg/mL. The suppression of fibronectin-binding activity by isoaaptamine (2) highlights its potential for the treatment of S. aureus infections via inhibition of SrtA activity. Our studies have identified a series of SrtA inhibitors, providing the basis for further development of potent inhibitors.
从海洋海绵Aaptos aaptos中分离出四种aaptamines(1-4),即1H-苯并[de][1,6]-萘啶生物碱,并评估了它们对分选酶A(SrtA)的抑制活性,该酶在金黄色葡萄球菌的细胞壁蛋白锚定和毒力中起关键作用。异aaptamine(2)是SrtA的有效抑制剂,IC(50)值为3.7±0.2微克/毫升。异aaptamine(2)对纤连蛋白结合活性的抑制突出了其通过抑制SrtA活性治疗金黄色葡萄球菌感染的潜力。我们的研究鉴定出了一系列SrtA抑制剂,为进一步开发强效抑制剂提供了基础。