Lysergamides
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Amides of lysergic acid are collectively known as lysergamides.[1][2][3]
Lysergamides, tabulated by structure
| Name | R1 | R6 | R2 | R3 |
|---|---|---|---|---|
| LSA / LAA | H | CH3 | H | H |
| DAM-57 | H | CH3 | CH3 | CH3 |
| Ergonovine | H | CH3 | CH(CH3)CH2OH | H |
| Methergine | H | CH3 | CH(CH2CH3)CH2OH | H |
| Methysergide | CH3 | CH3 | CH(CH2CH3)CH2OH | H |
| LAE-32 | H | CH3 | CH2CH3 | H |
| LSB | H | CH3 | CH(CH3)CH2CH3 | H |
| LSP | H | CH3 | CH(CH2CH3)CH2CH3 | H |
| DAL | H | CH3 | H2C=CH-CH2 | H2C=CH-CH2 |
| MIPLA | H | CH3 | CH(CH3)2 | CH3 |
| EIPLA | H | CH3 | CH(CH3)2 | CH2CH3 |
| LAMP | H | CH3 | CH2CH2CH3 | CH3 |
| LSD / LAD | H | CH3 | CH2CH3 | CH2CH3 |
| ETH-LAD | H | CH2CH3 | CH2CH3 | CH2CH3 |
| PARGY-LAD | H | HC≡C−CH2 | CH2CH3 | CH2CH3 |
| AL-LAD | H | H2C=CH-CH2 | CH2CH3 | CH2CH3 |
| PRO-LAD | H | CH2CH2CH3 | CH2CH3 | CH2CH3 |
| CYP-LAD | H | C3H5 | CH2CH3 | CH2CH3 |
| BU-LAD | H | CH2CH2CH2CH3 | CH2CH3 | CH2CH3 |
| ALD-52 | COCH3 | CH3 | CH2CH3 | CH2CH3 |
| MLD-41 | CH3 | CH3 | CH2CH3 | CH2CH3 |
| LSM-775 | H | CH3 | CH2CH2-O-CH2CH2 | |
| LPD-824 | H | CH3 | CH2CH2 CH2CH2 | |
| LSD-Pip | H | CH3 | CH2CH2 CH2CH2CH2 | |
| LA-SS-Az | H | CH3 | CH2(CHCH3)2CH2 |
[edit] References
- ^ Hofmann A. Psychotomimetic Drugs: Chemical and Pharmacological Aspects. Acta. Physiol. Pharmacol. Neerlandica. 1959;8:240-258.
- ^ US patent 2997470, Richard P. Pioch, "LYSERGIC ACID AMIDES", published 1956-03-05, issued 1961-08-22
- ^ David E. Nichols. LSD and Its Lysergamide Cousins. The Heffter Review of Psychedelic Research. 2001;2:80-87.
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