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FLUORETH-LAD

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
FLUORETH-LAD
Clinical data
Other namesTRALA-15; FE-LAD; 6-(2-Fluoroethyl)-6-nor-LSD; 6-(2-Fluoroethyl)-LAD;N,N-Diethyl-6-(2-fluoroethyl)-9,10-didehydroergoline-8β-carboxamide
Drug classSerotonin receptor modulator[1]
Identifiers
  • (6aR,9R)-N,N-diethyl-7-(2-fluoroethyl)-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
CAS Number
PubChemCID
Chemical and physical data
FormulaC21H26FN3O
Molar mass355.457 g·mol−1
3D model (JSmol)
  • CCN(CC)C(=O)[C@H]1CN([C@@H]2CC3=CNC4=CC=CC(=C34)C2=C1)CCF
  • InChI=1S/C21H26FN3O/c1-3-24(4-2)21(26)15-10-17-16-6-5-7-18-20(16)14(12-23-18)11-19(17)25(13-15)9-8-22/h5-7,10,12,15,19,23H,3-4,8-9,11,13H2,1-2H3/t15-,19-/m1/s1
  • Key:UYFDKYZWVLEHQH-DNVCBOLYSA-N

FLUORETH-LAD (TRALA-15),[2] orFE-LAD, also known as6-(2-fluoroethyl)-LAD or6-(2-fluoroethyl)-6-nor-LSD, is alysergamide derivative. It was first proposed byAlexander andAnn Shulgin in their bookTiHKAL,[3] but was never synthesised by Shulgin.

Synthesis and activity data for the compound were first reported in a 2022 patent by Matthias Grill, in which pharmacological testing showed it to have similar affinity to LSD at some targets such as the 5-HT1A and 5-HT2Aserotonin receptors, but much lower affinity at other targets such as 5-HT2C and atdopamine receptors, giving it comparatively greater selectivity compared to LSD.

Currently new lysergamide derivates are in the development phase atMiHKAL GmbH in Switzerland.[1]

See also

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References

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  1. ^abWO 2022/008627, Grill M, "Improved Method for the Production of Lysergic Acid Diethylamide (LSD) and Novel Derivatives thereof." 
  2. ^Trachsel D, et al. Lysergic acid derivatives with modified LSD-like action. US 2023/0414583
  3. ^TIHKAL #51: PRO-LAD

External links

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5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Ergolines
(incl.lysergines)
Clavines
(6,8-dimethylergolines)
Lysergamides
(lysergic acid amides)
Ergopeptines
(peptide ergolines)
Partial ergolines
Related compounds
Natural sources
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