Notoamides F−K, Prenylated Indole Alkaloids Isolated from a Marine-Derived Aspergillus sp.
- 18 November 2008
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Natural Products
- Vol. 71 (12), 2064-2067
- https://doi.org/10.1021/np800471y
Abstract
Six new prenylated indole alkaloids, named notoamides F−K (8−13), were isolated from a marine-derived Aspergillus sp. Their structures, including absolute configurations, were elucidated by spectroscopic methods. Notoamide I (11) showed weak cytotoxicity against HeLa cells with an IC50 value of 21 μg/mL.Keywords
This publication has 21 references indexed in Scilit:
- A Concise Total Synthesis of the Notoamides C and DAngewandte Chemie-International Edition, 2007
- Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine‐Derived Fungus, Aspergillus sp.Angewandte Chemie-International Edition, 2007
- Asperparaline A, a new paralytic alkaloid from Aspergillus japonicus JV-23Tetrahedron Letters, 1997
- Sclerotiamide: A New Member of the Paraherquamide Class with Potent Antiinsectan Activity from the Sclerotia of Aspergillus sclerotiorumJournal of Natural Products, 1996
- Remarkable, enantio-divergent biogenesis of brevianamide A and BJournal of the American Chemical Society, 1989
- Thin-Layer Chromatographic Enantiomeric Resolution via Ligand ExchangeAngewandte Chemie-International Edition, 1984
- The structure of paraherquamide, a toxic metabolite fromTetrahedron Letters, 1981
- Isolation and structure (X-ray analysis) of marcfortine A, a new alkaloid from Penicillium roquefortiJournal of the Chemical Society, Chemical Communications, 1980
- About metabolic products ofTetrahedron Letters, 1964
- The structure of cyclopenin and cyclopenol, metabolic products fromTetrahedron Letters, 1963