| Literature DB >> 24635109 |
Qing-Ai Liu1, Chang-Lun Shao1, Yu-Cheng Gu2, Mathias Blum2, Li-She Gan3, Kai-Ling Wang1, Min Chen1, Chang-Yun Wang1.
Abstract
Three new 14-membered resorcylic acid lactones, cochliomycins D-F, 1-3, and eight known analogues, 4-11, were isolated from the sea anemone-derived fungus Cochliobolus lunatus. Compounds 1-4 are diastereomers differing from each other by the absolute configurations of the 4',5'-diol chiral centers. The absolute configurations of 1-4 were established by the CD exciton chirality method and TDDFT ECD calculations. In antifouling assays, 1, 3-6, and 6a exhibited potent antifouling activities against the larval settlement of the barnacle Balanus amphitrite at nontoxic concentrations, with EC50 values ranging from 1.82 to 22.5 μg/mL. Noticeably, fungicide whole-plant assays indicated that 6 showed excellent activity on the Plasmopara viticola preventative test at 6 ppm and concentration-dependent activity on the Phytophthora infestans preventative application at 200, 60, and 20 ppm. Preliminary structure-activity relationships are also discussed.Entities:
Keywords: Cochliobolus lunatus; antifouling activity; fungicidal activity; resorcylic acid lactone; whole-plant assay
Year: 2014 PMID: 24635109 DOI: 10.1021/jf500248z
Source DB: PubMed Journal: J Agric Food Chem ISSN: 0021-8561 Impact factor: 5.279