Identity and Structure
| Chemical Name | MiPLA |
|---|---|
| Catalog Entity Type | Compound |
| Formula | C20H25N3O |
| Molar Mass | 323.440 g·mol−1 |
| CAS | 100768-08-9 |
| CAS Numbers and Substance Forms | 100768-08-9 Y |
| Synonyms | MiPLA; MIPLA; Lysergic acid methylisopropylamide; N-Methyl-N-isopropyllysergamide; LAMIDE; LA-Me/iso |
| IUPAC Name | (8β)-N-Isopropyl-N,6-dimethyl-9,10-didehydroergoline-8-carboxamide |
| InChI | InChI=1S/C20H25N3O/c1-12(2)23(4)20(24)14-8-16-15-6-5-7-17-19(15)13(10-21-17)9-18(16)22(3)11-14/h5-8,10,12,14,18,21H,9,11H2,1-4H3 |
| InChIKey | ROICYBLUWUMJFF-UHFFFAOYSA-N |
| SMILES | C4N(C)C1Cc2c[nH]c(ccc3)c2c3C1=CC4C(=O)N(C)C(C)C |
Chemical Identifiers
| PubChem CID | 57507938 |
|---|---|
| ChemSpider ID | 128916995 |
| UNII | AC6WQQ5Y4B |
Clinical Data
| Drug Class | Serotonin receptor modulator; 5-HT2A receptor agonist; Serotonergic psychedelic; Hallucinogen |
|---|---|
| Routes of Administration | Oral |
| ATC Code | None |
Pharmacokinetics
| Onset of Action | 20–40 minutes |
|---|---|
| Duration of Action | 4–6 hours |
Legal Status
| Legal Status (Wikipedia Source Text) | DE: NpSG (Industrial and scientific use only) UK: Under Psychoactive Substances Act US: Schedule I (isomer of LSD) Illegal in France |
|---|
Sources and Attribution
| Wikipedia Source URL | https://en.wikipedia.org/?curid=19913392 |
|---|---|
| Wikipedia Retrieval Date | 2026-10-21T20:05:08+00:00 |
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