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DOTFM-NDEPA

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Pharmaceutical compound
DOTFM-NDEPA
Clinical data
Other namesNDEPA-DOTFM; "Compound ko1"[1]
Drug class Possible serotonin 5-HT2A receptor modulator [1]
ATC code
  • None
Identifiers
CAS Number
Chemical and physical data
Formula C19H29F3N2O3
Molar mass 390.447 g·mol−1
3D model (JSmol)
  • C(F)(F)(F)C1C=C(C(=CC=1OC)CC(C)N(CCC(=O)N(CC)CC)[H])OC
  • InChI=1S/C19H29F3N2O3/c1-6-24(7-2)18(25)8-9-23-13(3)10-14-11-17(27-5)15(19(20,21)22)12-16(14)26-4/h11-13,23H,6-10H2,1-5H3
  • Key:XQPSNZUNPOQENQ-UHFFFAOYSA-N

DOTFM-NDEPA is a chemical compound of the phenethylamine, DOx, and NDEPA families.[1] It is the N-(N,N-diethylpropylamide) (NDEPA) derivative of the psychedelic drug DOTFM.[1] The drug can also be thought of as a derivative of DOTFM with an LSD-like N,N-diethylamide moiety.[1] A quantitative structure–activity relationship (QSAR) predicted that DOTFM-NDEPA would bind with high affinity to the serotonin 5-HT2A receptor.[1] Its predicted affinity (Ki) was 22 nM.[1] DOTFM-NDEPA was first described in the scientific literature by 1999.[1]

See also

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References

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  1. ^ a b c d e f g h Schulze-Alexandru M, Kovar KA, Vedani A (1999). "Quasi-atomistic Receptor Surrogates for the 5-HT2A Receptor: A 3D-QSAR Study on Hallucinogenic Substances" (PDF). Quantitative Structure-Activity Relationships. 18 (6): 548–560. doi:10.1002/(SICI)1521-3838(199912)18:6<548::AID-QSAR548>3.0.CO;2-B . ISSN 0931-8771 . Retrieved 6 July 2025.
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5-HT1
5-HT1A
  • Positive allosteric modulators: Oleamide
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT3 7
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
  • Negative allosteric modulators: Oleamide
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
Ergolines
(incl. lysergines)
Clavines
(6,8-dimethylergolines)
Lysergamides
(lysergic acid amides)
Ergopeptines
(peptide ergolines)
Partial ergolines
Related compounds
Natural sources


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