DOx
4-Substituted-2,5-dimethoxyamphetamines (DOx) is a chemical class of substituted amphetamine derivatives featuring methoxy groups at the 2- and 5- positions of the phenyl ring, and a substituent such as alkyl or halogen at the 4- position of the phenyl ring. Most compounds of this class are potent and long-lasting psychedelic drugs, and act as highly selective 5-HT2A, 5-HT2B, and 5-HT2C receptor partial agonists. A few bulkier derivatives such as DOAM have similarly high binding affinity for 5-HT2 receptors but instead act as antagonists, and so do not produce psychedelic effects.
The DOx family includes the following members:
As well as the following members with additional substitutions:
- 2,5-Dimethoxy-4-methyl-α-ethylphenethylamine (Ariadne)
- 2,5-Dimethoxy-4,N-dimethylamphetamine (Beatrice)
- 2,5-Dimethoxy-3,4-methylenedioxyamphetamine (DMMDA)
- 2,5-Dimethoxy-3,4-dimethylamphetamine (Ganesha)
- 2,5-Dimethoxy-3,4-trimethylenylamphetamine (G-3)
- 2,5-Dimethoxy-3,4-tetramethylenylamphetamine (G-4)
- 2,5-Dimethoxy-3,4-norbornylamphetamine (G-5)
- 2,5-Dimethoxy-4-iodo-N,N-dimethylamphetamine (IDNNA)
- 2,5-dimethoxy-4-bromo-N-methylamphetamine (Methyl-DOB)
- 2,3,4,5-Tetramethoxyamphetamine (TA, TeMA)
See also
References
External links
- PiHKAL ("Phenethylamines I Have Known And Loved") by Alexander "Sasha" Shulgin (1991)
- Psychotomimetic Drugs: Structure-Activity Relationships by Alexander "Sasha" Shulgin (1978)
5-HT1 |
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5-HT2 |
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5-HT3–7 |
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Human trace amine-associated receptor ligands | |||||||||||
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TAAR1 |
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TAAR2 |
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TAAR5 |
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† References for all endogenous human TAAR1 ligands are provided at List of trace amines
‡ References for synthetic TAAR1 agonists can be found at TAAR1 or in the associated compound articles. For TAAR2 and TAAR5 agonists and inverse agonists, see TAAR for references.
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Phenethylamines |
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Amphetamines |
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Phentermines |
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Cathinones |
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Phenylisobutylamines | |
Phenylalkylpyrrolidines | |
Catecholamines (and close relatives) |
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Miscellaneous |
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