Six new aurovertins (-) and a new citreoviridin derivative (), together with six known analogues (-), were isolated from the marine-derived sp. OUCMDZ-5930. Their structures were determined based on detailed spectroscopic analysis and ECD calculations. The putative nonenzymatic formation from citreoviridin to various aurovertins was presented, which was confirmed by chemical transformations. These results provide new insights into the formation mechanism of the 2,6-dioxabicyclo[3.2.1]octane ring system present in aurovertin-type natural products.
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http://dx.doi.org/10.1021/acs.jnatprod.4c01436 | DOI Listing |
J Nat Prod
January 2025
Key Laboratory of Marine Drugs, Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.
Six new aurovertins (-) and a new citreoviridin derivative (), together with six known analogues (-), were isolated from the marine-derived sp. OUCMDZ-5930. Their structures were determined based on detailed spectroscopic analysis and ECD calculations.
View Article and Find Full Text PDFChem Biodivers
February 2016
Department of Chemistry, Oregon State University, Corvallis, Oregon 97331, USA, (phone: +01 541-737-1690).
A comparative metabolomic study of a marine derived fungus (Aspergillus terreus) grown under various culture conditions is presented. The fungus was grown in eleven different culture conditions using solid agar, broth cultures, or grain based media (OSMAC). Multivariate analysis of LC/MS data from the organic extracts revealed drastic differences in the metabolic profiles and guided our subsequent isolation efforts.
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