Angewandte Chemie · 2007 · 27 citations · 13 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryMycologyStructure-activity RelationshipsFungal Natural Product BiosynthesisFungal Secondary MetabolitesMarine Bioactive CompoundsMarine Drug DiscoveryMarine Natural Product BiosynthesisMarine Natural ProductsBioactive Compounds From Marine FungiBioactive Fungal MetabolitesIndole AlkaloidsMarine Fungal MetabolitesMarine Fungal Natural ProductsMarine Fungal Secondary MetabolitesMarine Fungi As Drug SourcesMarine Secondary Metabolites
Aus dem Meer: Die Strukturen und Konfigurationen von vier neuen Indolalkaloiden aus dem aus Muscheln stammenden Pilz Aspergillus sp., den Notoamiden A–D, wurden bestimmt. Die Notoamide A–C sind moderat zytotoxisch gegen Krebszelllinien. Die Beziehung zwischen ihnen und anderen Metaboliten spricht dafür, dass der Pilz einen vielseitigen Biosyntheseweg nutzt. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2001/2007/z604381_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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The structure of paraherquamide, a toxic metabolite from
Mikio Yamazaki, Emi Okuyama, Makoto Kobayashi et al. · Tetrahedron Letters · 1981 · 202 citations
Pharmacy, Pharmacology, Toxicology +12