ETH-LAD
Chemistry
- Formula
- C21H27N3O
- Molar mass
- 337.5 g/mol
- IUPAC name
- (6aR,9R)-N,N,7-triethyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
- InChIKey
- MYNOUXJLOHVSMQ-DNVCBOLYSA-N
Chemistry from PubChem CID 44457783.
Also known as
- 65527-62-0
- N-EthylnorLSD
- N-Ethylnorlysergic acid N,N-diethylamide
- 21Z2736X9Q
- 6-Ethyl-6-nor-lysergic acid diethylamide
- 6-ETHYL-6-NOR-LSD
- DTXSID90215823
- (6aR,9R)-N,N,7-triethyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
Stereoisomers
3 distinct stereoisomers are registered for this structure.
- N-Ethylnorlysergic acid N,N-diethylamide this area CID 44457783
- (6aS,9R)-N,N,7-triethyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide CID 131706384
- (6aS,9S)-N,N,7-triethyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide CID 171042414
- ETH-LAD (solution) mixture CID 54098032
Attribution
David E. Nichols — first synthesis, 1985
The N(6)-ethyl analogue, from the same Hoffman & Nichols paper; also 2–3x more potent than LSD in the drug-discrimination assay.
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