ArticleAngewandte Chemie (International ed. in English)2016
Taichunamides: Prenylated Indole Alkaloids from Aspergillus taichungensis (IBT 19404).
Article in Angewandte Chemie (International ed. in English), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.
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Who cites it
23 citing papers in PubMed.
- Fungi and mycotoxins during conventional and improved postharvest processing and storage of local rice in Nigeria.Mycotoxin research · 2026Article
- Total Synthesis of (+)-Malbrancheamide B Employing a Bioinspired Strategy.Organic letters · 2026Article
- The Mutually Inspiring Biological and Chemical Synthesis of Fungal Bicyclo[2.2.2]diazaoctane Indole Alkaloids.Chemical reviews · 2025Review
- Seven New Species of Eurotiales (Ascomycota) Isolated from Tidal Flat Sediments in China.Journal of fungi (Basel, Switzerland) · 2023Article
- Recent Advances of Marine Natural Indole Products in Chemical and Biological Aspects.Molecules (Basel, Switzerland) · 2023Review
- A monograph ofStudies in mycology · 2022Article
- Antibacterial spirooxindole alkaloids fromFrontiers in microbiology · 2022Article
- 2,5-Diketopiperazines From a Sponge-Derived FungusFrontiers in microbiology · 2022Article
- Two New Quinazoline Derivatives from the Moss Endophytic Fungus Aspergillus sp. and Their Anti-inflammatory Activity.Natural products and bioprospecting · 2021Article
- Modular Approaches to Lankacidin Antibiotics.Journal of the American Chemical Society · 2020Article
- Polyhalonitrobutadienes as Versatile Building Blocks for the Biotargeted Synthesis of Substituted N-Heterocyclic Compounds.Molecules (Basel, Switzerland) · 2020Article
- Enzyme evolution in fungal indole alkaloid biosynthesis.The FEBS journal · 2020Review
- Classification ofStudies in mycology · 2020Article
- Facile one-pot synthesis of novelRSC advances · 2019Article
- Isolation of a new indoxyl alkaloid, Amoenamide B, fromTetrahedron letters · 2018Article
- Structural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi.Natural product reports · 2018Review
- New geranyl flavonoids from the leaves of Artocarpus communis.Journal of natural medicines · 2018Article
- Further Investigation of the Intermolecular Diels-Alder Cycloaddition for the Synthesis of Bicyclo[2.2.2]diazaoctane Alkaloids.The Journal of organic chemistry · 2017Article
- Structural Diversity and Biological Activities of the Cyclodipeptides from Fungi.Molecules (Basel, Switzerland) · 2017Review
- Enantioselective inhibitory abilities of enantiomers of notoamides against RANKL-induced formation of multinuclear osteoclasts.Bioorganic & medicinal chemistry letters · 2017Article
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7 authors.
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Abstract
Seven new prenylated indole alkaloids, taichunamides A-G, were isolated from the fungus Aspergillus taichungensis (IBT 19404). Taichunamides A and B contained an azetidine and 4-pyridone units, respectively, and are likely biosynthesized from notoamide S via (+)-6-epi-stephacidin A. Taichunamides C and D contain endoperoxide and methylsulfonyl units, respectively. This fungus produced indole alkaloids containing an anti-bicyclo[2.2.2]diazaoctane core, whereas A. protuberus and A. amoenus produced congeners with a syn-bicyclo[2.2.2]diazaoctane core. Plausible biosynthetic pathways to access these cores within the three species likely arise from an intramolecular hetero Diels-Alder reaction.
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