Identity and Structure
| Chemical Name | PRO-LAD |
|---|---|
| Catalog Entity Type | Compound |
| Formula | C22H29N3O |
| Molar Mass | 351.494 g·mol−1 |
| CAS | 65527-63-1 |
| CAS Numbers and Substance Forms | 65527-63-1 |
| Synonyms | PROLAD; 6-Propyl-6-nor-LSD; 6-Propyl-nor-LSD; 6-Propyl-6-norlysergic acid diethylamide; N,N-Diethyl-6-propyl-9,10-didehydroergoline-8β-carboxamide |
| IUPAC Name | (6aR,9R)-N,N-diethyl-7-propyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide |
| InChI | InChI=1S/C22H29N3O/c1-4-10-25-14-16(22(26)24(5-2)6-3)11-18-17-8-7-9-19-21(17)15(13-23-19)12-20(18)25/h7-9,11,13,16,20,23H,4-6,10,12,14H2,1-3H3/t16-,20-/m1/s1 |
| InChIKey | HZKYLVLOBYNKKM-OXQOHEQNSA-N |
| SMILES | CCN(CC)C(=O)[C@@H]2C=C1c3cccc4[nH]cc(C[C@H]1N(C2)CCC)c34 |
Chemical Identifiers
| PubChem CID | 44457803 |
|---|---|
| ChemSpider ID | 21106361 |
| UNII | RVR83W9XMC |
| ChEMBL ID | ChEMBL22258 |
| CompTox DTXSID | DTXSID50215824 |
Clinical Data
| Drug Class | Serotonin receptor modulator; Serotonin 5-HT2A receptor agonist; Serotonergic psychedelic; Hallucinogen |
|---|---|
| Routes of Administration | Oral |
Pharmacokinetics
| Onset of Action | ≤15 minutes |
|---|---|
| Duration of Action | 6–8 hours |
Legal Status
| Legal Status (Wikipedia Source Text) | DE: NpSG (Industrial and scientific use only) UK: Under Psychoactive Substances Act US: Analogue to a Schedule I/II drug but only if it is intended for human consumption Illegal in France |
|---|
Sources and Attribution
| Wikipedia Source URL | https://en.wikipedia.org/?curid=5837112 |
|---|---|
| Wikipedia Retrieval Date | 2026-10-21T20:07:22+00:00 |
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