Most Annonaceous acetogenins are characterized by between one and three THF ring(s) with one or two flanking hydroxyl group(s) in the center of a C32/34 fatty acid, and the terminal carboxylic acid is combined with a 2-propanol unit to form an α,Β-unsaturated γ-lactone. While many studies have addressed the properties and synthesis of natural acetogenins due to their attractive biological activities and unique structural features, a number of analogues have also been described. This review covers the design, synthesis, and biological evaluation of acetogenin analogues. © 2009 by the authors.
CITATION STYLE
Kojima, N., & Tanaka, T. (2009). Medicinal chemistry of annonaceous acetogenins: Design, synthesis, and biological evaluation of novel analogues. Molecules, 14(9), 3621–3661. https://doi.org/10.3390/molecules14093621
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