Fumigaclavine C
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Names | |
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IUPAC name
[(6aR,9S,10S)-7,9-Dimethyl-5-(2-methylbut-3-en-2-yl)-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinoline-10-yl] acetate
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Other names
SM-1; (8β,9β)-2-(1,1-Dimethyl-2-propenyl)-6,8-dimethylergolin-9-ol acetate
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Identifiers | |
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3D model (JSmol)
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ChEBI | |
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KEGG | |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C23H30N2O2 | |
Molar mass | 366.505 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Fumigaclavine C is an ergoline alkaloid produced by Aspergillus fumigatus.[1]
Both 8α and 8β diastereomers (epimers) were named fumigaclavine C in scientific literature.[2]
See also[]
- 9-Deacetoxyfumigaclavine C
- Fumigaclavine A
- Fumigaclavine B
- Fumigaclavine A dimethylallyltransferase
- Desformylflustrabromine
References[]
- ^ Ma, HY; Song, YC; Mao, YY; Jiang, JH; Tan, RX; Luo, L (2006). "Endophytic fungal metabolite fumigaclavine C causes relaxation of isolated rat aortic rings". Planta Medica. 72 (5): 387–92. doi:10.1055/s-2005-916235. PMID 16557450.
- ^ Wallwey, Christiane; Li, Shu-Ming (2011-03-01). "Ergot alkaloids: structure diversity, biosynthetic gene clusters and functional proof of biosynthetic genes". Natural Product Reports. 28 (3): 496–510. doi:10.1039/C0NP00060D. ISSN 1460-4752. PMID 21186384.
Categories:
- Ergolines
- Acetate esters
- Alkaloid stubs