| Identification | Back Directory | [Name]
chanoclavine | [CAS]
2390-99-0 | [Synonyms]
Secaclavine
(E)-2-Methyl-3-[(1,3,4,5-tetrahydro-4β-(methylamino)benz[cd]indol)-5α-yl]-2-propen-1-ol
(E)-2-Methyl-3-[(4R,5R)-1,3,4,5-tetrahydro-4-(methylamino)benz[cd]indol-5-yl]-2-propen-1-ol
2-Propen-1-ol, 2-methyl-3-[(4R,5R)-1,3,4,5-tetrahydro-4-(methylamino)benz[cd]indol-5-yl]-, (2E)- | [Molecular Formula]
C16H20N2O | [MOL File]
2390-99-0.mol | [Molecular Weight]
256.34 |
| Hazard Information | Back Directory | [Uses]
(R,R)-Chanoclavine is a modified ergot alkaloid produced by fungus. Stimulates dopamine receptors in the brain in rodents. | [Definition]
ChEBI:Chanoclavine-I is an organic tricyclic compound that is 1,3,4,5-tetrahydrobenzo[cd]indole which is substituted at position 4 by a methylamino group and at position 5 by a 3-hydroxy-2-methylprop-1-en-1-yl group (the 4R,5R,E diastereoisomer). It is a precursor of the tetracyclic ergolines agroclavine, elymoclavine and lysergic acid amide. It is an ergot alkaloid, a benzoindole, a secondary amino compound, a primary alcohol and an organic heterotricyclic compound. It is a conjugate base of a chanoclavine-I(1+). |
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