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6-MAPB

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
6-MAPB
Clinical data
Other names1-(Benzofuran-6-yl)-N-methylpropan-2-amine
Routes of
administration
Oral
Drug classMonoamine releasing agent;Serotonin5-HT1B receptoragonist
Legal status
Legal status
Identifiers
  • 1-(Benzofuran-6-yl)-N-methylpropan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC12H15NO
Molar mass189.258 g·mol−1
3D model (JSmol)
  • CC(NC)CC1=CC(OC=C2)=C2C=C1
  • InChI=1S/C12H15NO/c1-9(13-2)7-10-3-4-11-5-6-14-12(11)8-10/h3-6,8-9,13H,7H2,1-2H3
  • Key:QLAAURQYEAEHBO-UHFFFAOYSA-N

6-MAPB (1-(benzofuran-6-yl)-N-methylpropan-2-amine) is anentactogen of thebenzofuran family which is structurally related to6-APB andMDMA.[1][2][3][4] It is known to be aserotonin releasing agent and, unlike MDMA, apotentserotonin5-HT1B receptoragonist.[5] The drug is not known to have been widely sold as a "designer drug" but has been detected in analytical samples taken from individuals hospitalised after using drug combinations that included other benzofuran derivatives.[citation needed] 6-MAPB was first encountered as a noveldesigner drug in 2013 and described in thescientific literature in 2014.[6][7] It was banned in theUnited Kingdom in June 2013, along with 9 other related compounds which were thought to produce similar effects.[8]

Interactions

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See also:MDMA § Interactions,Trip killer § Antidotes of other hallucinogens, andMDMA/citalopram

See also

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References

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  1. ^Welter J, Brandt SD, Kavanagh P, Meyer MR, Maurer HH (May 2015)."Metabolic fate, mass spectral fragmentation, detectability, and differentiation in urine of the benzofuran designer drugs 6-APB and 6-MAPB in comparison to their 5-isomers using GC-MS and LC-(HR)-MS(n) techniques"(PDF).Analytical and Bioanalytical Chemistry.407 (12):3457–3470.doi:10.1007/s00216-015-8552-2.PMID 25711990.S2CID 5475974.
  2. ^Welter-Luedeke J, Maurer HH (February 2016). "New Psychoactive Substances: Chemistry, Pharmacology, Metabolism, and Detectability of Amphetamine Derivatives With Modified Ring Systems".Therapeutic Drug Monitoring.38 (1):4–11.doi:10.1097/FTD.0000000000000240.PMID 26327309.S2CID 20737913.
  3. ^Shimshoni JA, Winkler I, Golan E, Nutt D (January 2017). "Neurochemical binding profiles of novel indole and benzofuran MDMA analogues".Naunyn-Schmiedeberg's Archives of Pharmacology.390 (1):15–24.doi:10.1007/s00210-016-1297-4.hdl:10044/1/43622.PMID 27650729.S2CID 253741131.
  4. ^Brandt SD, Walters HM, Partilla JS, Blough BE, Kavanagh PV, Baumann MH (December 2020)."The psychoactive aminoalkylbenzofuran derivatives, 5-APB and 6-APB, mimic the effects of 3,4-methylenedioxyamphetamine (MDA) on monoamine transmission in male rats".Psychopharmacology.237 (12):3703–3714.doi:10.1007/s00213-020-05648-z.PMC 7686291.PMID 32875347.
  5. ^US 20230150963, Matthew Baggott, "Advantageous benzofuran compositions for mental disorders or enhancement", published 2023 May 18, assigned toTactogen 
  6. ^King LA (2014). "New phenethylamines in Europe".Drug Test Anal.6 (7–8):808–818.doi:10.1002/dta.1570.PMID 24574327.
  7. ^https://isomerdesign.com/bitnest/external/EMCDDA/New-Drugs-In-Europe-2013
  8. ^"Temporary class drug order report on 5-6APB and NBOMe compounds". UK Home Office. 4 Jun 2013. Retrieved2013-07-10.

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