Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

5-(2-Aminopropyl)indole

From Wikipedia, the free encyclopedia
(Redirected from5-API)
Chemical compound
Pharmaceutical compound
5-(2-Aminopropyl)indole
Clinical data
Other names5-API; 5-IT; PAL-571; PAL571; Indolylaminopropane; 3,4-Pyrrolo[b]amphetamine
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
Identifiers
  • 1-(1H-indol-5-yl)propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
ECHA InfoCard100.236.959Edit this at Wikidata
Chemical and physical data
FormulaC11H14N2
Molar mass174.247 g·mol−1
3D model (JSmol)
  • CC(N)Cc2cc1cc[nH]c1cc2
  • InChI=1S/C11H14N2/c1-8(12)6-9-2-3-11-10(7-9)4-5-13-11/h2-5,7-8,13H,6,12H2,1H3 checkY
  • Key:AULGMISRJWGTBA-UHFFFAOYSA-N checkY
  (verify)

5-(2-Aminopropyl)indole (5-API,5-IT,PAL-571)[1] is anindole andphenethylamine derivative with empathogenic effects. Its preparation was first reported byAlbert Hofmann in 1962.[2] It is adesigner drug that has been openly sold as arecreational drug by online vendors since 2011.[3]

Chemistry

[edit]

Although 5-IT is apositional isomer of thetryptamine drugαMT, the compound is not itself a tryptamine as the indole ring is substituted at the 5 position rather than at the 3 position. The compound is closer chemically to phenethylamine derivatives such as5-APB. This is reflected in the compound's effects when used as a drug, which are reportedly stimulating rather than psychedelic.

Pharmacology

[edit]

5-IT acts as aserotonin–norepinephrine–dopamine releasing agent (SNDRA) withEC50Tooltip half-maximal effective concentration values of 12.9 nM fordopamine, 13.3 nM fornorepinephrine, and 104.8 nM forserotonin, and is also anMAO-A inhibitor, with anIC50Tooltip half-maximal inhibitory concentration of 200 to 1,600 nM.[4][5][6] Additional molecular target data have also been reported for 5-IT, includingserotonin receptor interactions.[7]

Dosage and effects

[edit]

Alexander Shulgin wrote briefly about 5-IT inTiHKAL saying: "at 20 milligrams orally, [it] is a long-lived stimulant producing increased heart-rate, anorexia, diuresis, and slight hyperthermia for about twelve hours."[8] As 5-IT is not a tryptamine and thus not within the scope of the book, it is not discussed in any more detail than this.

The following symptoms can indicate 5-IT has been ingested:hyperthermia,tachycardia,increased blood pressure,dilated pupils (mydriasis),agitation, excessivesweating,jaw clenching,insomnia,disorientation,restlessness,anxiety, andtremor.[3] It is a MAOI, and when combined with a contraindicated substance, it can lead to death.

Deaths

[edit]

5-IT has been attributed to 14 deaths of people in Sweden since its discovery.[9][10] 5-IT was listed as the sole intoxicant in two cases but other drugs were also found in the twelve otherpost mortem examinations. The 14 deaths occurred between April and July 2012, but a definitive identification of 5-IT in the post-mortem samples was not made until July. All of the dead were young men aged between 20 and 30. Eleven non-fatal poisonings due to 5-IT also reportedly occurred during the same time period.[11]

Legality

[edit]
  • 5-IT is a positional isomer ofαMT, and as such is considered legally the same asαMT under theControlled Substances Act in the US. (The Federal Analog Act includes a clause concerning the effects of the substance as well.)
  • 5-IT was banned as atemporary class drug in June 2013, along with 9 other related compounds.[12] On March 5, 2014, the UK Home Office announced that 5-API would be made a class B drug on 10 June 2014 alongside every other benzofuran entactogen and many structurally related drugs.[13]
  • 5-IT is covered by the Australian analogue act as an analogue ofMDA "by the replacement of up to 2 carbocyclic or heterocyclic ring structures with different carbocyclic or heterocyclic ring structures".[14]
  • A formal application for 5-IT to be made illegal in Sweden was made on July 26, 2012, but did not come into effect immediately.
  • 5-IT was made illegal in Denmark on 30 September 2012.
  • 5-IT is anAnlage I controlled drug in Germany.
  • The European Commission published a proposal for a decision calling upon its member states to take measures to control 5-(2-aminopropyl)indole. It asked member states to introduce control measures and criminal penalties as provided under their national legislation covering psychotropic substances.[15]

See also

[edit]

References

[edit]
  1. ^Banks ML, Bauer CT, Blough BE, Rothman RB, Partilla JS, Baumann MH, Negus SS (June 2014)."Abuse-related effects of dual dopamine/serotonin releasers with varying potency to release norepinephrine in male rats and rhesus monkeys".Experimental and Clinical Psychopharmacology.22 (3):274–284.doi:10.1037/a0036595.PMC 4067459.PMID 24796848.
  2. ^FR 1344579, Hofmann, Albert; Troxler, Franz, "Nouveaux derives de l'indole et leur preparation" 
  3. ^abKatselou M, Papoutsis I, Nikolaou P, Spiliopoulou C, Athanaselis S (January 2015)."5-(2-aminopropyl)indole: a new player in the drama of 'legal highs' alerts the community".Drug and Alcohol Review.34 (1):51–7.doi:10.1111/dar.12136.PMID 24634984.
  4. ^Marusich JA, Antonazzo KR, Blough BE, Brandt SD, Kavanagh PV, Partilla JS, Baumann MH (February 2016)."The new psychoactive substances 5-(2-aminopropyl)indole (5-IT) and 6-(2-aminopropyl)indole (6-IT) interact with monoamine transporters in brain tissue".Neuropharmacology.101:68–75.doi:10.1016/j.neuropharm.2015.09.004.PMC 4681602.PMID 26362361.
  5. ^Herraiz T, Brandt SD (July–August 2014). "5-(2-Aminopropyl)indole (5-IT): a psychoactive substance used for recreational purposes is an inhibitor of human monoamine oxidase (MAO)".Drug Testing and Analysis.6 (7–8):607–613.doi:10.1002/dta.1530.hdl:10261/102667.PMID 24115740.
  6. ^Wagmann L, Brandt SD, Kavanagh PV, Maurer HH, Meyer MR (April 2017). "In vitro monoamine oxidase inhibition potential of alpha-methyltryptamine analog new psychoactive substances for assessing possible toxic risks".Toxicol Lett.272:84–93.doi:10.1016/j.toxlet.2017.03.007.PMID 28302559.
  7. ^Luethi D, Kolaczynska KE, Docci L, Krähenbühl S, Hoener MC, Liechti ME (May 2018). "Pharmacological profile of mephedrone analogs and related new psychoactive substances".Neuropharmacology.134 (Pt A):4–12.doi:10.1016/j.neuropharm.2017.07.026.PMID 28755886.
  8. ^Shulgin, Alexander (December 1997).Tihkal: A Continuation [Paperback]. Transform Press.ISBN 978-0-9630096-9-2. Retrieved2012-02-08.
  9. ^"Nätdrog dödade 14 unga män".Aftonbladet (in Swedish). 28 July 2012.
  10. ^Seetohul LN, Maskell PD, De Paoli G, Pounder DJ (August 2012)."Deaths associated with new designer drug 5-IT"(PDF).BMJ.345 e5625.doi:10.1136/bmj.e5625.PMID 22923530.S2CID 19956476.
  11. ^"Fem nya ämnen klassas som narkotika" (in Swedish). The Swedish National Institute of Public Health. Retrieved10 September 2015.
  12. ^"Temporary class drug order report on 5-6APB and NBOMe compounds". UK Home Office. 4 Jun 2013. Retrieved2013-07-11.
  13. ^UK Home Office (2014-03-05)."The Misuse of Drugs Act 1971 (Ketamine etc.) (Amendment) Order 2014". UK Government. Retrieved2014-03-11.
  14. ^"Criminal Code Act 1995"(PDF). Australian Government. 2009-08-05. Retrieved2012-02-08.PAGE 503
  15. ^"COM(2013) 436 final"(PDF). European Commission. 2013-06-25. Retrieved2013-06-26.
Adamantanes
Adenosine antagonists
Alkylamines
Ampakines
Arylcyclohexylamines
Benzazepines
Cathinones
Cholinergics
Convulsants
Eugeroics
Oxazolines
Phenethylamines
Phenylmorpholines
Piperazines
Piperidines
Pyrrolidines
Racetams
Tropanes
Tryptamines
Others
DRAsTooltip Dopamine releasing agents
NRAsTooltip Norepinephrine releasing agents
SRAsTooltip Serotonin releasing agents
Others
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Non-specific
AAADTooltip Aromatic L-amino acid decarboxylase
MAOTooltip Monoamine oxidase
Phenethylamines
(dopamine,epinephrine,
norepinephrine)
PAHTooltip Phenylalanine hydroxylase
THTooltip Tyrosine hydroxylase
DBHTooltip Dopamine beta-hydroxylase
PNMTTooltip Phenylethanolamine N-methyltransferase
COMTTooltip Catechol-O-methyl transferase
Tryptamines
(serotonin,melatonin)
TPHTooltip Tryptophan hydroxylase
AANATTooltip Serotonin N-acetyl transferase
ASMTTooltip Acetylserotonin O-methyltransferase
Histamine
HDCTooltip Histidine decarboxylase
HNMTTooltip Histamine N-methyltransferase
DAOTooltip Diamine oxidase
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
Stimulants
Depressants
Hallucinogens
Entactogens
Psychiatric drugs
Others
Retrieved from "https://en.wikipedia.org/w/index.php?title=5-(2-Aminopropyl)indole&oldid=1311715657"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp