Dipropyltryptamine
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N,N-Dipropyltryptamine (DPT) is a psychedelic drug and entheogen belonging to the tryptamine family.[1] Use as a designer drug has been documented by law enforcement officials since as early as 1968.[2] However, potential therapeutic use was not investigated until the 1970s.[3] It is found either as a crystalline hydrochloride salt or as an oily or crystalline base. It has not been found to occur endogenously. It is a close structural homologue of dimethyltryptamine and diethyltryptamine.
Use and effects
Doses ranges of DPT of 100 to 250Template:Nbspmg (but up to 500Template:Nbspmg) orally, 100Template:Nbspmg smoked, 15 to 125Template:Nbspmg intramuscularly, and 12 to 36Template:Nbspmg intravenously have been described.[1][4] Its duration is 2 to 4Template:Nbsphours orally but can last up to 12Template:Nbsphours with high doses.[1]
While DPT is chemically similar to dimethyltryptamine (DMT), its psychoactive effects have been said to be markedly different.[5] On the other hand, others have reported similarities to DMT, for instance in terms of intensity.[1]
Side effects
Side effects of DPT may include nausea, numbness of the tongue or throat, pupil dilation, increased heart rate, dizziness, anxiety, panic, confusion, paranoia, delusions, and seizures (uncommon).Script error: No such module "Unsubst".
The use of DPT has been implicated in at least one death due to seizures,[6] although details are lacking and the drug has not officially been established as the sole cause of death.
Interactions
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Pharmacology
| Target | Affinity (Ki, nM) | Species |
|---|---|---|
| 5-HT1A | 31.8–1,641 (Ki) 274–>10,000 (Template:Abbrlink) 99% (Template:Abbrlink) |
Human Human |
| 5-HT1B | 854–8,081 (Ki) 1,210 (EC50) |
Human Human |
| 5-HT1D | 619 | Human |
| 5-HT1E | 2,338 | Human |
| 5-HT2A | 3.0–2,579 (Ki) 26.1–943 (EC50) 85–97% (Emax) |
Human Human Human |
| 5-HT2B | 42 | Human |
| 5-HT2C | 281–3,500 (Ki) 444 (EC50) 93% (Emax) |
Human |
| 5-HT3 | >10,000 | Human |
| 5-HT4 | ND | ND |
| 5-HT5A | 4,373 | Human |
| 5-HT6 | 4,543 | Human |
| 5-HT7 | 284 | Human |
| D1 | >10,000 | Human |
| D2 | 9,249 | Human |
| D3 | 1,361 | Human |
| D4 | 2,014 | Human |
| D5 | >10,000 | Human |
| α1A | 881 | Human |
| α1B | 443 | Human |
| α1D | ND | ND |
| α2A | 458 | Human |
| α2B | 339 | Human |
| α2C | 514 | Human |
| β1–β2 | >10,000 | Human |
| H1 | 125 | Human |
| H2–H4 | >10,000 | Human |
| M1–M5 | >10,000 | Human |
| I1 | 340 | Human |
| σ1 | 397 | Human |
| σ2 | 2,917 | Human |
| Template:Abbrlink | 157 (Ki) 157–23,000 (Template:Abbrlink) >100,000 (EC50) |
Human Human Rat |
| Template:Abbrlink | >10,000 (Ki) 2,900–3,202 (IC50) >100,000 (EC50) |
Human Human Rat |
| Template:Abbrlink | 1,500 (Ki) 2,218–9,100 (IC50) >100,000 (EC50) |
Human Human Rat |
| Notes: The smaller the value, the more avidly the drug binds to the site. Refs: [7][8][9][10][11][12][13] | ||
Studies on rodents have found that the effectiveness with which a selective 5-HT2A receptor antagonist blocks the behavioral actions of this compound strongly suggests that the 5-HT2A receptor is an important site of action for DPT, but the modulatory actions of a 5-HT1A receptor antagonist also imply a 5-HT1A-mediated component to the actions of DPT.[14]
DPT produces the head-twitch response, a behavioral proxy of psychedelic-like effects, in rodents.[4]
Chemistry
DPT changes Ehrlich's reagent violet and causes the marquis reagent to turn yellow.[15]
History
DPT was first described in the scientific literature by 1959.[16][17][18]
Society and culture
Religious use
DPT is used as a religious sacrament by the Temple of the True Inner Light, a New York City offshoot of the Native American Church. The Temple believes DPT and other entheogens are physical manifestations of God.[19]
Legal status
Sweden
DPT is illegal in Sweden as of 26 January 2016.[20]
United Kingdom
DPT is a Class A drug in the United Kingdom, making it illegal to possess or distribute.
United States
DPT is not scheduled at the federal level in the United States,[21] but it could be considered an analog of 5-MeO-DiPT, DMT, or DET, in which case purchase, sale, or possession could be prosecuted under the Federal Analogue Act.
Florida
"DPT (N,N-Dipropyltryptamine)" is a Schedule I controlled substance in the state of Florida making it illegal to buy, sell, or possess in Florida.[22]
Maine
DPT is a Schedule I controlled substance in the state of Maine making it illegal to buy, sell, or possess in Maine.
References
External links
- DPT - Isomer Design
- TiHKAL entry
- DPT entry in TiHKAL • info
- A DPT Primer by Toad
- Erowid Experience Vault
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- ↑ Florida Statutes – Chapter 893 – DRUG ABUSE PREVENTION AND CONTROL