Abstract
Two phenylpropanoids from Bupleurum fruticosum (Apiaceae/ Umbelliferae) were shown to inhibit the transcriptional activity induced by PMA or TNFα of an NF-κB-controlled reporter gene. Western blot experiments indicated that the phenylpropanoids did not prevent 1κBα degradation, suggesting that their molecular target is at a post-1KB degradation level. Both compounds prevented cytokine (IL-1, IL-6, TNF, IL-8) release and prostaglandin E2 synthesis.
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Brernner, P., Tang, S., Birkmayer, H., Fiebich, B. L., Muñoz, E., Marquez, N., … Heinrich, M. (2004). Phenylpropanoid NF-κB inhibitors from Bupleurum fruticosum. Planta Medica, 70(10), 914–918. https://doi.org/10.1055/s-2004-832616
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