Lophophine
From Wikipedia, the free encyclopedia
| Lophophine | |
|---|---|
 |
|
| IUPAC name | 2-(7-Methoxy-benzo[1,3]dioxol-5-yl)-ethylamine |
| Other names | 3-Methoxy-4,5-methylenedioxyphenethylamine 2-(7-Methoxy-1,3-benzodioxol-5-yl)ethanamine |
| Identifiers | |
| CAS number | [1484-85-1] |
| SMILES | NCCc1cc2OCOc2c(c1)OC |
| Properties | |
| Molecular formula | C10H13NO3 |
| Molar mass | 211.258 g/mol |
| Melting point |
164-164.5 °C (hydrochloride) |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
|
Lophophine, homomyristicylamine, (r 3-methoxy-4,5-methylendioxyphenethylamine is an homologue of MMDA. It is also related to mescaline and Alexander Shulgin suggests it could be a natural component in the peyote cactus because it is the only logical chemical intermediate for the biosynthesis of several of tetrahydroisoquinolines known to be present in the cactus. Lophophine produces hallucinogenic, psychedelic, and entheogenic effects that are similar to mescaline.
Contents |
[edit] Chemistry
Lophophine is in a class of compounds commonly known as phenethylamines, and the full chemical name is 2-(7-methoxy-1,3-benzodioxol-5-yl)ethanamine.
[edit] Effects
Little is known about the psychopharmacological effects of lophophine, but it does appear to have qualitative and quantitative effects that resemble mescaline. Shulgin reports in Mescaline: The Chemistry and Pharmacology of its Analogs that lophophine is active at 150-250 mg. He states at these dosages that the action of this base is quite similar to that of mescaline; there is a peaceful elevation of mood, euphoria, enhancement of visual perception, and the generation of eyes-closed imagery. At dosages above 300 mg, visual distortions that resemble those of mescaline begin to appear. He also notes that in contrast to mescaline, little nausea is produced from lophophine ingestion.
[edit] Pharmacology
The mechanism that produces the hallucinogenic and entheogenic effects of lophophine is unknown. Although structure-activity relationships mean that it is likely to be caused by 5-HT2A receptor agonism - similar to other psychedelic drugs such as LSD and mescaline.
[edit] Dangers
The toxicity of lophophine is not known.
[edit] Legality
Lophophine is unscheduled and unregulated in the United States, however because of its close similarity in structure and effects to MDA and MMDA, possession and sale of lophophine may be subject to prosecution under the Federal Analog Act.
[edit] See also
[edit] External links
- Lophophine entry in PiHKAL
- Psychotomimetic Drugs: Structure-Activity Relationships.
- Mescaline: The Chemistry and Pharmacology of its Analogs.
|
|||||
|
|||||
