Agroclavine
Names | |
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IUPAC name
(6aR,10aR)-7,9-Dimethyl-4,6,6a,7,8,10a-hexahydroindolo[4,3-fg]quinoline | |
Other names
6,8-Dimethyl-8,9-didehydroergoline; 8,9-Didehydro-6,8-dimethylergoline | |
Identifiers | |
548-42-5 | |
3D model (Jmol) | Interactive image |
ChEBI | CHEBI:2519 |
ChEMBL | ChEMBL449081 |
ChemSpider | 66176 |
ECHA InfoCard | 100.008.135 |
PubChem | 73484 |
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Properties | |
C16H18N2 | |
Molar mass | 238.33 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Agroclavine belongs to the group of ergot alkaloids, such as ergotamine.[1] Historically, the main use of argoclavine was to oxidize it to elymoclavine, which can then be used for ergot-based drug synthesis.
References
- ↑ Bhattacharji, S.; Birch, A. J.; Brack, A.; Hofmann, A.; Kobel, H.; Smith, D. C. C.; Smith, Herchel; Winter J. (1962). "Biosynthesis. XXVII. The biosynthesis of ergot alkaloids". Journal of the Chemical Society: 421–425.
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