Abstract
Fungicidal activity of 36 natural and synthetic sesquiterpene lactones with guaianolide, trans, trans-germacranolide, cis, cis-germacranolide, melampolide, and eudesmanolide carbon skeletons was evaluated against the phytopathogenic fungi Colletotrichum acutatum, C. fragariae, C. gloeosporioides, Fusarium oxysporum, Botrytis cinerea, and Phomopsis sp. Dose-response data for the active compounds dehydrozaluzanin C, dehydrocostuslactone, 5α-hydroxydehydrocostuslacone, costunolide, and zaluzanin C are presented. A new 96-well microbioassay procedure for fast and easy evaluation of antifungal activity was used to compare these compounds with commercial fungicide standards. Some structure-activity conclusions are also presented. (C) 2000 Elsevier Science Ltd.
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Wedge, D. E., Galindo, J. C. G., & Macías, F. A. (2000). Fungicidal activity of natural and synthetic sesquiterpene lactone analogs. Phytochemistry, 53(7), 747–757. https://doi.org/10.1016/S0031-9422(00)00008-X
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