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Names | |
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IUPAC name
6,8-Dimethyl-8,9-didehydroergoline
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Systematic IUPAC name
(6aR,10aR)-7,9-Dimethyl-4,6,6a,7,8,10a-hexahydroindolo[4,3-fg]quinoline | |
Other names
8,9-Didehydro-6,8-dimethylergoline
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Identifiers | |
3D model (
JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.008.135 |
PubChem
CID
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UNII | |
CompTox Dashboard (
EPA)
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Properties | |
C16H18N2 | |
Molar mass | 238.334 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Agroclavine belongs to the group of ergot alkaloids, which also includes ergotamine. [1] Historically, the main use of agroclavine was in the synthesis of ergot-based drugs; agroclavine can be oxidized to elymoclavine, which then undergoes further processing. [2]
![]() | |
Names | |
---|---|
IUPAC name
6,8-Dimethyl-8,9-didehydroergoline
| |
Systematic IUPAC name
(6aR,10aR)-7,9-Dimethyl-4,6,6a,7,8,10a-hexahydroindolo[4,3-fg]quinoline | |
Other names
8,9-Didehydro-6,8-dimethylergoline
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.008.135 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C16H18N2 | |
Molar mass | 238.334 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Agroclavine belongs to the group of ergot alkaloids, which also includes ergotamine. [1] Historically, the main use of agroclavine was in the synthesis of ergot-based drugs; agroclavine can be oxidized to elymoclavine, which then undergoes further processing. [2]