Journal of Natural Products · 2011 · 21 citations · 9 references
Life SciencesBiologyMicrobiologyBioorganic ChemistryMycologyPlant Molecular BiologyFungal Natural Product BiosynthesisFungal Secondary MetabolitesPhenylpropanoid BiosynthesisAntibacterial PropertiesAntimicrobial Marine CompoundsBioactive Compounds From Marine FungiClaisen CondensationClaisen RearrangementHydrolysisMarine Fungal Natural ProductsSpectroscopic Characterization
Marianins A (1) and B (2), two new prenylated phenylpropanoids, were isolated from the culture extract of the fungus Mariannaea camptospora. Structures of marianins were elucidated by interpretation of NMR and other spectroscopic data. 1 is a 5-methylcoumarin bearing two prenyloxy groups, while 2 is an orcinol derivative substituted with a 3,3-dimethyl-4-pentenoyl chain. 2 is possibly derived from 1 through a Claisen rearrangement of the prenyl group, followed by lactone hydrolysis and decarboxylation. These compounds showed weak antibacterial activity against Micrococcus luteus.
9
Paecilomyces and Some Allied Hyphomycetes
Transactions of the British Mycological Society · 1975 · 496 citations
Life Sciences, Biology, Microbiology +10
Bioactive Substances from Insect Pathogenic Fungi
Masahiko Isaka, Prasat Kittakoop, Kanyawim Kirtikara et al. · Accounts of Chemical Research · 2005 · 190 citations
Houping Liu, Margaret Skinner, Bruce L. Parker et al. · Journal of Economic Entomology · 2002 · 82 citations
Emily M. Stocking, Robert M. Williams, Juan F. Sanz‐Cervera · Journal of the American Chemical Society · 2000 · 56 citations