Cytotoxic and antimicrobial drimane meroterpenoids from a fungus of the Stictidaceae (Ostropales, Ascomycota)
Author:
Funder
National Cancer Institute
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Chemical Diversity of Metabolites from Fungi, Cyanobacteria, and Plants Relative to FDA-Approved Anticancer Agents
2. Meroterpenoids from Neosetophoma sp.: A Dioxa[4.3.3]propellane Ring System, Potent Cytotoxicity, and Prolific Expression
3. Discovery of Anticancer Agents of Diverse Natural Origin
4. Cytotoxic terpenoids from Dasyscyphus niveus
5. Dasyscyphin F (1): Yellow powder; = +27 (c = 0.1, CH3OH); UV (CH3OH) λmax (log ε) 254 (3.63); 1H NMR (CDCl3, 400 MHz) and 13C NMR (CDCl3, 100 MHz) see Table 1 and Fig. S2; HRESIMS m/z 341.2125 [M-H]- (calcd. for C22H29O3, m/z 341.2122, 0.8 ppm).
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1. Isolation, (bio)synthetic studies and evaluation of antimicrobial properties of drimenol-type sesquiterpenes of Termitomyces fungi;Communications Chemistry;2023-04-24
2. Natural sesquiterpene quinone/quinols: chemistry, biological activity, and synthesis;Natural Product Reports;2023
3. Metabolomics-Guided Comparison of Pollen and Microalgae-Based Artificial Diets in Honey Bees;Journal of Agricultural and Food Chemistry;2022-07-26
4. Biosynthesis of Fungal Drimane‐Type Sesquiterpene Esters;Angewandte Chemie International Edition;2021-10
5. Biosynthesis of Fungal Drimane‐Type Sesquiterpene Esters;Angewandte Chemie;2021-10
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