ArticleOrganic letters2015
Isolation of notoamide S and enantiomeric 6-epi-stephacidin A from the fungus Aspergillus amoenus: biogenetic implications.
Article in Organic letters, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.
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Who cites it
16 citing papers in PubMed.
- Four new Cyclohexenone with antibacterial activity from the coral-derived fungus Aspergillus flavus.Natural products and bioprospecting · 2026Article
- The Mutually Inspiring Biological and Chemical Synthesis of Fungal Bicyclo[2.2.2]diazaoctane Indole Alkaloids.Chemical reviews · 2025Review
- Taxonomy ofStudies in mycology · 2022Article
- Flavin-Dependent Monooxygenases NotI and NotI' Mediate Spiro-Oxindole Formation in Biosynthesis of the Notoamides.Chembiochem : a European journal of chemical biology · 2020Article
- Enzyme evolution in fungal indole alkaloid biosynthesis.The FEBS journal · 2020Review
- Enantioselective assembly of multi-layerNational science review · 2020Article
- Notoamide-type alkaloid induced apoptosis and autophagyRSC advances · 2019Article
- Isolation of a new indoxyl alkaloid, Amoenamide B, fromTetrahedron letters · 2018Article
- Prenylated indole alkaloids from co-culture of marine-derived fungi Aspergillus sulphureus and Isaria felina.The Journal of antibiotics · 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
- 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
- Isolation of amoenamide A and five antipodal prenylated alkaloids fromTetrahedron letters · 2017Article
- Taichunamides: Prenylated Indole Alkaloids from Aspergillus taichungensis (IBT 19404).Angewandte Chemie (International ed. in English) · 2016Article
- Marine Indole Alkaloids.Marine drugs · 2015Review
Corrections and comments
- Erratum issued
Authors and funding
9 authors.
Funding
Abstract
Notoamide S has been hypothesized to be a key biosynthetic intermediate for characteristic metabolites stephacidin A, notoamide B, and versicolamide B in Aspergillus sp. but has not yet been isolated. The isolation of notoamide S and an enantiomeric mixture of 6-epi-stephacidin A enriched with the (-)-isomer from Aspergillus amoenus is reported. The presence of (+)-versicolamide B suggests that the fungus possesses only the oxidase, which converts (+)-6-epi-stephacidin A into (+)-Versicolamide B, but not for (-)-6-epi-Stephacidin A.
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