5-APB

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5-APB
5-APB2DACS.svg
Ball-and-stick model of the 5-APB molecule
Systematic (IUPAC) name
5-(2-Aminopropyl)benzofuran
Clinical data
Legal status
Identifiers
CAS Number 286834-81-9 N
ATC code none
PubChem CID: 9837232
ChemSpider 8012953 YesY
Synonyms 1-Benzofuran-5-ylpropan-2-amine
Benzo fury
Benzofury
Chemical data
Formula C11H13NO
Molecular mass 175.23 g/mol
  • CC(N)CC1=CC(C=CO2)=C2C=C1
  • InChI=1S/C11H13NO/c1-8(12)6-9-2-3-11-10(7-9)4-5-13-11/h2-5,7-8H,6,12H2,1H3 YesY
  • Key:VKUMKUZDZWHMQU-UHFFFAOYSA-N YesY
 NYesY (what is this?)  (verify)

5-APB (5-(2-aminopropyl)benzofuran, 1-benzofuran-5-ylpropan-2-amine, benzofury) is a triple monoamine reuptake inhibitor with Ki values of 180, 265 and 811 nM for NET, DAT and SERT respectively as well as being a potent agonist for the 5-HT2A and 5-HT2B receptors (Ki of 14nM at 5-HT2B).[1][2] This agonism for 5-HT2B makes it likely that 5-APB would be cardiotoxic with long term use, as seen in other 5-HT2B agonists such as fenfluramine and MDMA. The subjective effects and structure-activity relationship suggest that 5-APB is also a monoamine releasing agent.[citation needed]

5-APB is commonly found as the succinate and hydrochloride salt. The hydrochloride salt is 10% more potent by mass and doses should be adjusted accordingly.

5-APB is also an agonist of the 5-HT2C receptor [3] as well as a triple monoamine reuptake inhibitor.[2] It has been sold as a designer drug since 2010.[4]

Detection

A forensic standard of 5-APB is available, and the compound has been posted on the Forendex website of potential drugs of abuse.[5] The US Department of Justice and DEA have also conducted studies concerning the detection of 5-APB.[6]

Effects

Users describe effects as euphoric. Largely, effects reported were similar to that of the drug MDA but not as strong.[citation needed] Recreational use of 5-APB has been associated with death in combination with other drugs.[7][8]

Legality

On March 5, 2014 the UK Home Office announced that 6-APB would be made a class B drug on 10 June 2014 alongside every other benzofuran entactogen and many structurally related drugs.[9]

See also

References

  1. ↑ Dawson P, Opacka-Juffry J, Moffatt JD, Daniju Y, Dutta N, Ramsey J, Davidson C. The effects of benzofury (5-APB) on the dopamine transporter and 5-HT2-dependent vasoconstriction in the rat. Progress in Neuropsychopharmacology and Biological Psychiatry. 2014 Jan 3;48:57-63. doi: 10.1016/j.pnpbp.2013.08.013. PMID 24012617
  2. ↑ 2.0 2.1 Lua error in package.lua at line 80: module 'strict' not found.
  3. ↑ US patent 7045545, Karin Briner et al, "Aminoalkylbenzofurans as serotonin (5-HT(2c)) agonists", published 2000-01-19, issued 2006-16-03 
  4. ↑ EMCDDA–Europol 2010 Annual Report on the implementation of Council Decision 2005/387/JHA
  5. ↑ Southern Association of Forensic Scientists, http://forendex.southernforensic.org/index.php/detail/index/1135
  6. ↑ USDOJ/DEA, http://www.justice.gov/dea/pr/microgram-journals/2011/mj8-2_62-74.pdf
  7. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  8. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  9. ↑ Lua error in package.lua at line 80: module 'strict' not found.
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