| Literature DB >> 17716892 |
Kyoung Hwa Jang1, Soon-Chun Chung, Jongheon Shin, So-Hyoung Lee, Tae-Im Kim, Hyi-Seung Lee, Ki-Bong Oh.
Abstract
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.Entities:
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Year: 2007 PMID: 17716892 DOI: 10.1016/j.bmcl.2007.08.007
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823