Abstract
Damsin (1) is a natural pseudoguaianolide sesquiterpene that inhibits NF-κB, a protein complex that controls the transcription of DNA in mammalian cells, and has a potential for standing model for the development of new anti-cancer lead structures. In order to do a preliminary structure-activity study and improve the anti-cancer activity, fourteen derivatives and analogs were prepared and evaluated. These were chosen to represent both structural diversity and structural novelty. The importance of α methylene-γ-lactone moiety for the anti-cancer activity was confirmed, even though other features in the scaffold were shown to be important for the activity. In some cases a new substitution negatively affected the initial activity, however, two analogues, indolo [3,2-c]-4-desoxydamsin (5) and ambrosin (6), were found to be more potent.
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CITATION STYLE
Villagomez, R., Collado, J. A., Muñoz, E., Almanza, G., & Sterner, O. (2014). Natural and Semi-Synthetic Pseudoguaianolides as Inhibitors of NF-κB. Journal of Biomedical Science and Engineering, 07(10), 833–847. https://doi.org/10.4236/jbise.2014.710083
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