Article ID Journal Published Year Pages File Type
1374988 Bioorganic & Medicinal Chemistry Letters 2008 4 Pages PDF
Abstract

Acetogenins of the Annonaceae are strong inhibitors of mitochondrial complex I but discrepancies in the structure/activity relationships pled the search for other targets within the whole cell proteome. Combining hemisynthetic work, Cu-catalyzed Huisgen cycloaddition and proteomic techniques we have identified new putative protein targets of squamocin ruling out the previously accepted ‘complex I dogma’. These results give new insights into the mechanism of action of these potent neurotoxic molecules.

Graphical abstractCombining hemisynthetic work, Cu-catalyzed Huisgen cycloaddition and proteomic techniques, we have identified new putative protein targets of squamocin ruling out the previously accepted ‘complex I dogma’ in the annonaceous acetogenin series.Figure optionsDownload full-size imageDownload as PowerPoint slide

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Physical Sciences and Engineering Chemistry Organic Chemistry
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