| Verifiedrevid: | 447115140 |
| Drug Name: | α-Ethyltryptamine |
| Inn: | Etryptamine |
| Usan: | Etryptamine |
| Tradename: | Monase |
| Routes Of Administration: | Oral |
| Class: | Entactogen |
| Legal Br: | F2 |
| Legal Br Comment: | [1] |
| Legal Ca: | Schedule III |
| Legal Us: | Schedule I |
| Legal Uk: | Class A |
| Legal De: | Anlage I |
| Legal Un: | P I |
| Metabolism: | Hydroxylation |
| Metabolites: | • 6-Hydroxy-αET (inactive) |
| Onset: | 0.5–1.5hours |
| Elimination Half-Life: | ~8hours |
| Duration Of Action: | 6–8hours (100–150mg) |
| Excretion: | Urine (majority) |
| Cas Number: | 2235-90-7 |
| Cas Supplemental: | (acetate) (hydrochloride) |
| Atc Prefix: | None |
| Pubchem: | 8367 |
| Pubchemsubstance: | 46507084 |
| Drugbank: | DB01546 |
| Chemspiderid: | 8064 |
| Unii: | GR181O3R32 |
| Chebi: | 134838 |
| Chembl: | 1619758 |
| Kegg: | D04092 |
| Synonyms: | alpha-Ethyltryptamine; αET; AET; α-ET; Etryptamine; PAL-125; 3-(2-Aminobutyl)indole; 3-Indolylbutylamine; U-17312E; U17312E; Ro 3-1932; NSC-63963; NSC-88061 |
| Iupac Name: | 1-(1H-indol-3-yl)butan-2-amine |
| C: | 12 |
| H: | 16 |
| N: | 2 |
| Smiles: | CCC(N)CC1=CNC2=CC=CC=C12 |
| Stdinchi: | 1S/C12H16N2/c1-2-10(13)7-9-8-14-12-6-4-3-5-11(9)12/h3-6,8,10,14H,2,7,13H2,1H3 |
| Stdinchikey: | ZXUMUPVQYAFTLF-UHFFFAOYSA-N |
| Melting Point: | 222 |
| Melting High: | 223 |
α-Ethyltryptamine (αET, AET), also known as etryptamine, is an entactogen and stimulant drug of the tryptamine family.[2] [3] [4] It was originally developed and marketed as an antidepressant under the brand name Monase by Upjohn in the 1960s before being withdrawn due to toxicity.[5]
Side effects of αET include facial flushing, headache, gastrointestinal distress, insomnia, irritability, appetite loss, and sedation, among others. A rare side effect of αET is agranulocytosis.[6] αET acts as a releasing agent of serotonin, norepinephrine, and dopamine, as a weak serotonin receptor agonist, and as a weak monoamine oxidase inhibitor. It may also produce serotonergic neurotoxicity. αET is a substituted tryptamine and is closely related to α-methyltryptamine (αMT) and other α-alkylated tryptamines.
αET was first described in 1947. It was used as an antidepressant for about a year around 1961. The drug started being used recreationally in the 1980s and several deaths have been reported. αET is a controlled substance in various countries, including the United States and United Kingdom. There has been renewed interest in αET, for instance as an alternative to MDMA, with the development of psychedelics and entactogens as medicines in the 2020s.
αET was previously used medically as an antidepressant and "psychic energizer" to treat people with depression. It was used for this indication under the brand name Monase.
αET was available pharmaceutically as the acetate salt under the brand name Monase in the form of 15mg oral tablets.[7]
αET is reported to have entactogen and weak psychostimulant effects. Euphoria, increased energy, openness, and empathy have been specifically reported. Unlike αMT and other tryptamines, αET is not reported to have psychedelic or hallucinogenic effects. The drug is described as less stimulating and intense than MDMA ("ecstasy") but as otherwise having entactogenic effects resembling those of MDMA. The dose of αET used recreationally has been reported to be 100 to 160mg, its onset of action has been reported to be 0.5 to 1.5hours, and its duration of action at the preceding doses is described as 6 to 8hours. Rapid tolerance to repeated administration of αET has been described.
Side effects of αET at antidepressant doses have included facial flushing, headache, gastrointestinal distress, insomnia, irritability, and sedation. Additional side effects of αET at recreational doses have included appetite loss and feelings of intoxication. Feelings of lethargy and sedation can occur once the drug wears off.
As with many other serotonin releasing agents, toxicity, such as serotonin syndrome, can occur when excessive doses are taken or when combined with certain drugs such as monoamine oxidase inhibitors (MAOIs).[8] Several deaths have been associated with recreational use of αET.[9]
Rarely, agranulocytosis has occurred with prolonged administration of αET at antidepressant doses and has been said to have resulted in several cases and/or deaths.
αET has been administered in clinical studies at doses of up to 300mg per day.[10] An approximate but unconfirmed 700mg dose resulted in fatal hyperthermia and agitated delirium in one case. LD50 doses of αET for various species have been studied and described. Treatment of αET intoxication or overdose is supportive. Severe and potentially life-threatening hyperthermia may occur. Serotonergic toxicity associated with serotonergic agents like αET can be managed with benzodiazepines and with the serotonin receptor antagonist cyproheptadine.[11]
Similarly to αMT, αET is a releasing agent of serotonin, norepinephrine and dopamine, with serotonin being the primary neurotransmitter affected.[12] It is about 10-fold more potent in inducing serotonin release than in inducing dopamine release and about 28-fold more potent in inducing serotonin release than in inducing norepinephrine release. The (+)-enantiomer of αET, (+)-αET, is a serotonin–dopamine releasing agent (SDRA) and is one of the few such agents known. It is about 1.7-fold more potent in inducing serotonin release than in inducing dopamine release, about 17-fold more potent in inducing serotonin release than in inducing norepinephrine release, and is about 10-fold more potent in inducing dopamine release than in inducing norepinephrine release.
In addition to acting as a monoamine releasing agent, αET acts as a serotonin receptor agonist. It is known to act as a weak partial agonist of the serotonin 5-HT2A receptor (> 10,000nM; Emax = 21%). (–)-αET is inactive as a 5-HT2A receptor agonist at concentrations of up to 10μM, whereas (+)-αET is a 5-HT2A receptor agonist with an EC50 value of 1,250nM and an Emax value of 61%. αET has also been found to have weak affinity for the 5-HT1, 5-HT1E, 5-HT1F, and 5-HT2B receptors.
| Compound | Monoamine release (nM) | 5-HT2A receptor agonism | ||||
|---|---|---|---|---|---|---|
| (nM) | Emax (%) | |||||
| 32.6 ± 2.6 | 164 ± 16 | 716 ± 46 | 7.36 ± 0.56 | 104 ± 4 | ||
| 44.4 ± 5.3 | >10,000 | >10,000 | ||||
| 114 ± 15 | >10,000 | 4,166 ± 317 | 38.3 ± 0.81 | 83 ± 0.4 | ||
| 21.7 ± 1.0 | 78.6 ± 4.0 | 112 ± 6 | 23.1 ± 2.4 | 103 ± 3 | ||
| αET | 23.2 ± 1.7 | 232 ± 17 | 640 ± 76a | >10,000 | 21 ± 11 | |
| (–)-αET | 54.9 ± 7.8 | 654 ± 50 | 3,670 ± 1,190a | >10,000 | – | |
| (+)-αET | 34.7 ± 4.9 | 57.6 ± 3.1 | 592 ± 97a | 1,250 ± 310 | 61 ± 8 | |
| 56.6 ± 2.1 | 376 ± 16 | 77.4 ± 3.4 | ||||
| Notes: The smaller the value, the more strongly the compound produces the effect. Footnotes: a = αET, (–)-αET, and (+)-αET were norepinephrine partial releasers with Emax values of 78%, 75%, and 71%, respectively. Refs: [13] [14] | ||||||
αET is a weak monoamine oxidase inhibitor (MAOI).[15] It is specifically a selective and reversible inhibitor of monoamine oxidase A (MAO-A). An value of 260μM in vitro and 80 to 100% inhibition of MAO-A at a dose of 10mg/kg in rats in vivo have been reported.[16] αET is described as slightly more potent as an MAOI than dextroamphetamine. Both enantiomers of αET have similar activity as MAOIs, whereas αET's major metabolite 6-hydroxy-αET is inactive. The relatively weak MAOI actions of αET have been considered unlikely to be involved in its stimulant, antidepressant, and other psychoactive effects by certain sources.
The stimulant effects of αET have been said to lie primarily in (–)-αET, whereas hallucinogenic effects have been said to be present in (+)-αET. However, these claims appear to be based on animal drug discrimination studies and are not necessarily in accordance with functional studies. Generalization to may have been anomalous and due to the serotonin-releasing actions of αET rather than due to serotonin 5-HT2A receptor activation and associated psychedelic effects. Accordingly, αET does not produce the head-twitch response in rodents, unlike known psychedelics. In addition, clear hallucinogenic effects of αET have never been documented in humans even at high doses, although the individual enantiomers of αET have never been studied in humans.
αET has been found to produce serotonergic neurotoxicity similar to that of MDMA and para-chloroamphetamine (PCA) in rats.[17] This has included long-lasting reductions in serotonin levels, 5-hydroxyindoleacetic acid (5-HIAA) levels, and serotonin uptake sites in the frontal cortex and hippocampus. The dosage of αET employed was 8doses of 30mg/kg by subcutaneous injection with doses spaced by 12-hour intervals. There are prominent species differences in the neurotoxicity of monoamine releasing agents.[18] [19] Primates appear to be more susceptible to the damage caused by serotonergic neurotoxins like MDMA than rodents.
The absorption of αET appears to be rapid. It has a relatively large volume of distribution. The drug undergoes hydroxylation to form the major metabolite 6-hydroxy-αET (3-(2-aminobutyl)-6-hydroxyindole). This metabolite is inactive. αET is eliminated primarily in urine and a majority of a dose is excreted in urine within 12 to 24hours. Its elimination half-life is approximately 8hours.
αET, also known as 3-(2-aminobutyl)indole, is a substituted tryptamine and α-alkyltryptamine derivative. Analogues of αET include α-methyltryptamine (αMT) and other substituted α-alkylated tryptamines like 5-MeO-αET, 5-chloro-αMT (PAL-542), and 5-fluoro-αET (PAL-545).
αET was first described in the scientific literature in 1947.[20] The enantiomers of αET were first individually described in 1970.
Originally believed to exert its effects predominantly via monoamine oxidase inhibition, αET was developed during the 1960s as an antidepressant by Upjohn chemical company in the United States under the generic name etryptamine and the brand name Monase, but was withdrawn from potential commercial use due to incidence of idiosyncratic agranulocytosis in several patients. It was on the market for about a year, around 1961, and was given to more than 5,000patients, before being withdrawn. αET was usually used as an antidepressant at doses of 30 to 40mg/day (but up to 75mg/day), which are lower than the doses that have been used recreationally.
αET gained limited recreational popularity as a designer drug with MDMA-like effects in the 1980s. Subsequently, in the United States it was added to the Schedule I list of illegal substances in 1993 or 1994.
Etryptamine is the formal generic name of the drug and its and .[21] In the case of the acetate salt, its generic name is etryptamine acetate and this is its . Etryptamine was used pharmaceutically as etryptamine acetate. Etryptamine is much more well-known as alpha-ethyltryptamine or α-ethyltryptamine (abbreviated as αET, α-ET, or AET). Other synonyms of αET and/or its acetate salt include 3-(2-aminobutyl)indole, 3-indolylbutylamine, PAL-125, U-17312E, Ro 3-1932, NSC-63963, and NSC-88061, as well as its former brand name Monase.[22] [23]
αET has been used as a recreational drug since the 1980s.[24] Purported street names include Trip, ET, Love Pearls, and Love Pills.
αET is a Schedule I controlled substance in the United States and a Class A controlled substance in the United Kingdom.
Besides depression, αET has been studied in people with schizophrenia and other conditions.