Compounds.

Similarities

The following is a set of comparisons to understand the properties of this compound. This is still higly experimental and is still under active development. Please refer to our series of blog posts to fully understand our approach and its limitations. This information is for informational purposes only and should not be construed as medical advice.

Most structurally similar compounds. The percentage is a measure of how structurally similar those molecules are, which is often strongly correlated with their effects.

1

3,2,5-DOET

2

homo-TMA-3

3

4,2,6-DOET

4

4,3,5-DOET

48.8%

5

6-Me-2,3-DOM

48.8%

6

3-Me-2,6-DOM

48.8%

7

dopr

DOPR

48.8%

8

3-Me-2,4-DOM

48.8%

9

2-Me-3,4-DOM

48.8%

10

DOM-5ETO

IRIS (psychedelic)

48.8%

11

DOM-2ETO

48.8%

12

3,4,5-DOET

48.7%

13

5,2,3-DOET

48.7%

14

doet

DOET

1-(4-ethyl-2,5-dimet...

2,5-Dimethoxy-4-ethy...

48.7%

15

2,4,5-DOET

48.7%

16

5,2,4-DOET

48.7%

17

ψ-DOM

1-(2,6-dimethoxy-4-m...

Psi-DOM

48.7%

18

homo-DMA

48.7%

19

homo-TMA-6

48.7%

20

5-Me-2,3-DOM

48.7%

21

5-Me-3,4-DOM

48.7%

22

4-Me-3,5-DOM

48.7%

23

6-Me-2,4-DOM

48.7%

24

homo-TMA-2

48.7%

25

3-DOM

48.7%

26

2-Me-3,5-DOM

48.7%

27

5-DOM

48.6%

28

2-DOM

48.6%

29

DOM

dom

DOM

2,5-Dimethoxy-4-meth...

DOM

DOM

2,5-Dimethoxy-4-meth...

48.6%

30

homo-DOM

0.0%
Similarities computed based on affinities of molecules with selected proteins docking site.
- List of compounds which have the most similar docking sites affinities. The percentage is a measure of how similar the binding affinities of the molecules are, which should be a proxy to how similarly they interact with the brain.
  
  1
  
  AMPT
  
  Metyrosine
  
  Metirosine
  
  2
  
  Theacrine
  
  theacrine
  
  Theacrine
  
  Theacrine
  
  3
  
  N-Me-2,6-DMPEA
  
  4
  
  3-MT
  
  3-Methoxytyramine
  
  84.7%
  
  5
  
  2-ADN
  
  2-Amino-1,2-dihydron...
  
  84.7%
  
  6
  
  N-Methyl-7,8-dihydro...
  
  84.7%
  
  7
  
  3-Hydroxy-4-methylam...
  
  84.7%
  
  8
  
  N-Methylmetanephrine
  
  84.7%
  
  9
  
  MDAI
  
  mdai
  
  5,6-MDAI
  
  MDAI
  
  MDAI
  
  84.7%
  
  10
  
  Baclofen
  
  baclofen
  
  Baclofen
  
  Baclofen
  
  84.7%
  
  11
  
  2C-3a
  
  84.6%
  
  12
  
  oMPP
  
  Ortho-Methylphenylpi...
  
  84.6%
  
  13
  
  MHAT
  
  84.5%
  
  14
  
  NCS-382
  
  84.5%
  
  15
  
  GAMMA
  
  84.4%
  
  16
  
  N,N-Me-2,6-DMPEA
  
  84.4%
  
  17
  
  β-Me-DHPEA
  
  84.4%
  
  18
  
  2-AT
  
  1,2,3,4-Tetrahydro-n...
  
  2-Aminotetralin
  
  84.3%
  
  19
  
  Norbaeocystin
  
  Norbaeocystin
  
  80.0%
- List of compounds which have the most similar docking sites affinities and have also high dopamine receptor interactions, but now using addictive data predicted by a Machine Learning model. In practive this one is slightly more reliable than the other approach. This is thus a proxy to how much this molecule stimulates the dopamine receptors.
  
  1
  
  1P-LSD
  
  1p-lsd
  
  1P-LSD
  
  1P-LSD
  
  1P-LSD
  
  2
  
  Haloperidol
  
  Haloperidol
  
  Haloperidol
  
  Haloperidol
  
  Haloperidol
  
  3
  
  JWH-018
  
  JWH-018
  
  1-Pentyl-3-(1-naphth...
  
  JWH-018
  
  4
  
  Salvinorin A
  
  Salvinorin A
  
  Salvinorin A
  
  Salvinorin A
  
  Salvinorin A
  
  40.0%
  
  5
  
  Buprenorphine
  
  buprenorphine
  
  (18R)-17-(Cyclopropy...
  
  Buprénorphine
  
  Buprenorphine
  
  Buprenorphine
  
  40.0%
  
  6
  
  MiPLA
  
  MIPLA
  
  Methylisopropyllyser...
  
  40.0%
  
  7
  
  Cinolazepam
  
  cinolazepam
  
  Cinolazepam
  
  Cinolazepam
  
  Cinolazepam
  
  40.0%
  
  8
  
  JWH-073
  
  JWH-073
  
  1-Butyl-3-(1-naphtho...
  
  JWH-073
  
  39.9%
  
  9
  
  THJ-018
  
  THJ-018
  
  THJ-018
  
  39.9%
  
  10
  
  5F-AKB48
  
  5f-akb48
  
  5F-APINACA
  
  5F-AKB48
  
  5F-APINACA
  
  39.9%
  
  11
  
  Salvinorin B methoxy...
  
  Methoxymethyl salvin...
  
  Salvinorin B methoxy...
  
  Salvinorin B methoxy...
  
  39.9%
  
  12
  
  THC-O
  
  Δ9-THC acetate
  
  THC-O-acetate
  
  39.9%
  
  13
  
  Risperidone
  
  Risperidone
  
  Risperidone
  
  Risperidone
  
  Risperidone
  
  39.9%
  
  14
  
  4-AcO-DMT
  
  4-aco-dmt
  
  4-AcO-DMT
  
  4-AcO-DMT
  
  O-Acetylpsilocin
  
  39.8%
  
  15
  
  25B-NBOH
  
  25b-nboh
  
  25B-NBOH
  
  25B-NBOH
  
  25B-NBOH
  
  39.7%
  
  16
  
  THJ-2201
  
  THJ-2201
  
  THJ-2201
  
  39.7%
  
  17
  
  bzp
  
  BZP
  
  Benzylpiperazine
  
  39.7%
  
  18
  
  4-fea
  
  4-FEA
  
  39.6%
  
  19
  
  Pregabalin
  
  pregabalin
  
  Pregabalin
  
  Pregabalin
  
  Prégabaline
  
  Pregabalin
  
  Pregabalin
  
  39.5%
  
  20
  
  ethketamine
  
  Ethketamine
  
  N-Ethylnorketamine
  
  39.4%
  
  21
  
  Alpha-GPC
  
  Choline alfoscerate
  
  Glycerophosphorylcho...
  
  39.2%
  
  22
  
  brotizolam
  
  Brotizolam
  
  Brotizolam
  
  39.1%
  
  23
  
  2C-T-2
  
  2c-t-2
  
  2C-T-2
  
  2C-T-2
  
  2C-T-2
  
  39.0%
  
  24
  
  ALD-52
  
  ald-52
  
  1-Acetyl-LSD
  
  ALD-52
  
  ALD-52
  
  38.6%
  
  25
  
  Benzydamine
  
  benzydamine
  
  Benzydamine
  
  Benzydamine
  
  Benzydamine
  
  Benzydamine
  
  38.2%
  
  26
  
  Naloxone
  
  3,14-Dihydroxy-17-(p...
  
  Naloxone
  
  Naloxone
  
  Naloxone
  
  38.1%
  
  27
  
  Diphenidine
  
  diphenidine
  
  Diphenidine
  
  Diphénidine
  
  Diphenidine
  
  38.1%
  
  28
  
  rolicyclidine
  
  PCPy
  
  Rolicyclidine
  
  Rolicyclidine
  
  Rolicyclidine
  
  38.1%
  
  29
  
  3-Me-PCP
  
  3-Me-PCP
  
  3-Methyl-PCP
  
  37.8%
  
  30
  
  2-Aminoindane
  
  2-ai
  
  2-AI
  
  2-Aminoindane
  
  37.3%
- Binding affinities with a list of 34 predefined docking sites. Those affinities are used to compute the interactions similarities.
  
  AF-A5X5Y0
  
  AF-O95264
  
  AF-P08588
  
  AF-P08908
  
  AF-P13945
  
  AF-P18089
  
  AF-P21728
  
  AF-P21918
  
  AF-P25100
  
  AF-P28221
  
  AF-P28566
  
  AF-P46098
  
  AF-Q9Y2T6
  
  P08913_6KUX
  
  P14416_6CM4
  
  P18825_6KUW
  
  P21917_5WIU
  
  P28222_4IAR
  
  P28223_6WGT
  
  P28335_6BQH
  
  P35462_3PBL
  
  P41595_4IB4
Interaction of this molecule with metabolism ?

Reactions that metabolize this molecule

Dephosphorylation of phosphate monoester

Product:

Metabolite: InChI=1S/C11H14...

Enzymes: EC 3.1.3.1, EC 3.1.3.2

Hydroxylation of non-terminal aliphatic carbon adjacent to aromatic ring

Product:

InChI=1S/C11H15N2O5P...

Enzymes: CYP1A2, CYP2C8, CYP2C9, CYP2D6, CYP3A4

Aromatic hydroxylation of fused benzene ring

Product:

InChI=1S/C11H15N2O5P...

Enzymes: CYP1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP2E1, CYP3A4

Aromatic hydroxylation of fused benzene ring

Product:

InChI=1S/C11H15N2O5P...

Enzymes: CYP1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP2E1, CYP3A4

N-Dealkylation of acyclic secondary amine

Product:

Metabolite: InChI=1S/C10H13...

Enzymes: CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4

N-Dealkylation of acyclic secondary amine

Product:

Metabolite: Methylamine

Enzymes: CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4

N-Dealkylation of acyclic secondary amine

Product:

InChI=1S/C10H10NO5P/...

Enzymes: CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4

Reactions that metabolism produce from this molecule

Dephosphorylation of phosphate monoester

Product:

Metabolite: InChI=1S/C11H14...

Enzymes: EC 3.1.3.1, EC 3.1.3.2

Hydroxylation of non-terminal aliphatic carbon adjacent to aromatic ring

Product:

InChI=1S/C11H15N2O5P...

Enzymes: CYP1A2, CYP2C8, CYP2C9, CYP2D6, CYP3A4

Aromatic hydroxylation of fused benzene ring

Product:

InChI=1S/C11H15N2O5P...

Enzymes: CYP1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP2E1, CYP3A4

Aromatic hydroxylation of fused benzene ring

Product:

InChI=1S/C11H15N2O5P...

Enzymes: CYP1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP2E1, CYP3A4

N-Dealkylation of acyclic secondary amine

Product:

Metabolite: InChI=1S/C10H13...

Enzymes: CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4

N-Dealkylation of acyclic secondary amine

Product:

Metabolite: Methylamine

Enzymes: CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4

N-Dealkylation of acyclic secondary amine

Product:

InChI=1S/C10H10NO5P/...

Enzymes: CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A4

Baeocystin

Baeocystin

Similarities

3,2,5-DOET

homo-TMA-3

4,2,6-DOET

4,3,5-DOET

6-Me-2,3-DOM

3-Me-2,6-DOM

dopr

DOPR

3-Me-2,4-DOM

2-Me-3,4-DOM

DOM-5ETO

IRIS (psychedelic)

DOM-2ETO

3,4,5-DOET

5,2,3-DOET

doet

DOET

1-(4-ethyl-2,5-dimet...

2,5-Dimethoxy-4-ethy...

2,4,5-DOET

5,2,4-DOET

ψ-DOM

1-(2,6-dimethoxy-4-m...

Psi-DOM

homo-DMA

homo-TMA-6

5-Me-2,3-DOM

5-Me-3,4-DOM

4-Me-3,5-DOM

6-Me-2,4-DOM

homo-TMA-2

3-DOM

2-Me-3,5-DOM

5-DOM

2-DOM

DOM

dom

DOM

2,5-Dimethoxy-4-meth...

DOM

DOM

2,5-Dimethoxy-4-meth...

homo-DOM

AMPT

Metyrosine

Metirosine

Theacrine

theacrine

Theacrine

Theacrine

N-Me-2,6-DMPEA

3-MT

3-Methoxytyramine

2-ADN

2-Amino-1,2-dihydron...

N-Methyl-7,8-dihydro...

3-Hydroxy-4-methylam...

N-Methylmetanephrine

MDAI

mdai

5,6-MDAI

MDAI

MDAI

Baclofen

baclofen

Baclofen

Baclofen

2C-3a

oMPP

Ortho-Methylphenylpi...

MHAT

NCS-382

GAMMA

N,N-Me-2,6-DMPEA

β-Me-DHPEA

2-AT

1,2,3,4-Tetrahydro-n...