Natural Product Research · 2019 · 33 citations · 12 references
PharmacyBotanyMedicinal ChemistryBioorganic ChemistryDrug DiscoveryOrganic ChemistryAlkaloid BiosynthesisFungal Natural Product BiosynthesisFungal Secondary MetabolitesMarine Drug DiscoveryMarine Natural ProductsAbsolute Configuration AssignmentAbsolute Configuration DeterminationBioactive Compounds From Marine FungiIndole AlkaloidsIndole ChemistryMarine Fungal Natural ProductsPlant AlkaloidsRelative Configuration Determination
A new prenylated indole alkaloid, named paraherquamide J (1), together with four known compounds (2–5), were isolated from the mangrove rhizosphere soil-derived fungus Penicillium janthinellum HK1-6. The planar structure and relative configuration of 1 were determined by detailed analysis of the spectroscopic data especially the NOESY spectrum. The absolute configuration of 1 was determined by ECD spectra. Compound 2 was first isolated as a natural product and named as paraherquamide K. All isolated metabolites were evaluated for their antibacterial, topoisomerase I (topo I) inhibitory activities and lethality towards brine shrimp Artemia salina.
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Brine Shrimp: A Convenient General Bioassay for Active Plant Constituents
Brian F. Meyer, N. R. Ferrigni, J. E. Putnam et al. · Planta Medica · 1982 · 4.8K citations
Christopher G. Pierce, Priya Uppuluri, Floyd L. Wormley et al. · Nature Protocols · 2008 · 823 citations
A Microwell Cytotoxicity Assay using<i>Artemia salina</i>(Brine Shrimp)
Pablo N. Solís, Colin W. Wright, Margaret Lavinia Anderson et al. · Planta Medica · 1993 · 522 citations
Pharmacy, Pharmacology, Toxicology +12