Natural and Semi-Synthetic Pseudoguaianolides as Inhibitors of NF-κB

dc.contributor.authorRodrigo Villagomez
dc.contributor.authorJuan A. Collado
dc.contributor.authorEduardo Muñóz
dc.contributor.authorGiovanna R. Almanza
dc.contributor.authorOlov Sterner
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T14:50:13Z
dc.date.available2026-03-22T14:50:13Z
dc.date.issued2014
dc.descriptionCitaciones: 10
dc.description.abstractDamsin (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.
dc.identifier.doi10.4236/jbise.2014.710083
dc.identifier.urihttps://doi.org/10.4236/jbise.2014.710083
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/48833
dc.language.isoen
dc.publisherScientific Research Publishing
dc.relation.ispartofJournal of Biomedical Science and Engineering
dc.sourceLund University
dc.subjectMoiety
dc.subjectChemistry
dc.subjectStereochemistry
dc.subjectStructure–activity relationship
dc.subjectTranscriptional activity
dc.subjectTranscription (linguistics)
dc.subjectCancer cell
dc.subjectTranscription factor
dc.subjectBiochemistry
dc.subjectCancer
dc.titleNatural and Semi-Synthetic Pseudoguaianolides as Inhibitors of NF-κB
dc.typearticle

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