| Literature DB >> 15214798 |
Vasudha Sharma1, Theresa A Lansdell, Guangyi Jin, Jetze J Tepe.
Abstract
We describe herein the synthesis and biological activity of two indoloazepines that are structurally related to the marine sponge metabolite hymenialdisine. The natural product hymenialdisine was found to be a potent inhibitor of interleukin-2 (IC(50) = 2.4 microM) and tumor necrosis factor alpha (IC(50) = 1.4 microM) production. One of the hymenialdisine derived indoloazepines was found to also inhibit interleukin-2 (IC(50) = 3.5 microM) and tumor necrosis factor alpha (IC(50) = 8.2 microM) production.Entities:
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Year: 2004 PMID: 15214798 DOI: 10.1021/jm040013d
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446