1P-ETH-LAD

1P-ETH-LAD is an N1-propionyl derivative of ETH-LAD, a lysergamide with an N6-ethyl substitution. It combines the N1-acyl modification found in compounds such as 1P-LSD with the altered ergoline structure of ETH-LAD. The compound has been analytically characterised, and human-serum experiments indicate that it can be converted to ETH-LAD. Its human pharmacology, however, has not been established in controlled studies.

Chemistry and identification

ETH-LAD is N6-ethyl-6-norlysergic acid diethylamide. In 1P-ETH-LAD, a propionyl group is added at the N1 position. This means the compound differs from 1P-LSD at the N6 position as well as from ETH-LAD at N1.

The 2017 analytical study used GC-MS, low- and high-resolution electrospray MS, GC-solid-state infrared spectroscopy, HPLC-DAD and NMR to characterise ETH-LAD and 1P-ETH-LAD. The work made analytical data available for a compound that had appeared on the new psychoactive substance market without a prior detailed scientific description (Brandt and colleagues, 2017).

Conversion to ETH-LAD

When 1P-ETH-LAD was incubated with human serum at 37 °C, ETH-LAD formed over the observation period. The parent compound was still detectable after 24 hours in that in-vitro experiment. The authors therefore suggested that 1P-ETH-LAD may act as a prodrug for ETH-LAD, while noting that the study did not establish the process in living humans.

A broader metabolism investigation of LSD-based new psychoactive substances included 1P-ETH-LAD among nine lysergamides. It found that N-dealkylation and hydroxylation were common pathways across the group, with CYP1A2 and CYP3A4 contributing to initial metabolism (Wagmann and colleagues, 2019).

Pharmacology and reported effects

The human pharmacology of 1P-ETH-LAD has not been examined in a substantial controlled study. Its proposed conversion to ETH-LAD provides a plausible route to lysergamide activity, but does not establish the extent of conversion, the contribution of the intact parent compound or the subjective effects in people.

Descriptions of ETH-LAD or 1P-LSD offer comparisons, but do not establish the effects of 1P-ETH-LAD.

Toxicology and research gaps

Most published evidence concerns analytical chemistry and in-vitro metabolism. There is no well-characterised human toxic range, controlled dependence assessment or long-term safety study specific to 1P-ETH-LAD. Clinical interpretation is further complicated when products are identified from blotter material without biological confirmation.

Related lysergamides

1P-ETH-LAD is related to ETH-LAD, 1P-LSD, 1cP-LSD and 1cP-AL-LAD. Its combination of N1-propionyl and N6-ethyl substitutions distinguishes it from the other compounds in this group.

1P-ETH-LAD Products

Chemical structure of 1P-ETH-LAD

1P-ETH-LAD liquid

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Chemical structure of 1P-ETH-LAD

1P-ETH-LAD pellets

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Chemical structure of 1P-ETH-LAD

1P-ETH-LAD blotters

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Reference information

Scientific Data

Structured reference fields associated with this compound.

Identity and Structure

Chemical Name1P-ETH-LAD
Catalog Entity TypeCompound
FormulaC24H31N3O2
Molar Mass393.531 g·mol−1
CAS2230715-45-2
CAS Numbers and Substance Forms2230715-45-2
Synonyms1-Propionyl-ETH-LAD; 1-Propionyl-6-ethyl-6-nor-LSD
IUPAC Name(6aR,9R)-N,N-Diethyl-7-ethyl-4-propanoyl-6,6a,8,9-tetrahydroindolo[4,3-fg]quinoline-9-carboxamide
InChIInChI=1S/C24H31N3O2/c1-5-22(28)27-15-16-13-21-19(18-10-9-11-20(27)23(16)18)12-17(14-26(21)8-4)24(29)25(6-2)7-3/h9-12,15,17,21H,5-8,13-14H2,1-4H3/t17-,21-/m1/s1
InChIKeyMLOFCBXSOAYCIF-DYESRHJHSA-N
SMILESCCC(=O)N1C=C2C[C@@H]3C(=C[C@H](CN3CC)C(=O)N(CC)CC)C4=C2C1=CC=C4

Chemical Identifiers

PubChem CID119025859
ChemSpider ID52085137
UNIIHA76076A0R
CompTox DTXSIDDTXSID301016300

Clinical Data

Drug ClassSerotonergic psychedelic; Hallucinogen
Routes of AdministrationOral

Legal Status

Legal Status (Wikipedia Source Text)DE: NpSG (Industrial and scientific use only)
UK: Under Psychoactive Substances Act
Illegal in France

Sources and Attribution

Wikipedia Retrieval Date2026-10-21T18:52:14+00:00