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4C-B

From Wikipedia, the free encyclopedia
Pharmaceutical compound
4C-B
Clinical data
Other names4C-DOB; DOB-B; 4-Bromo-2,5-dimethoxy-α-ethylphenethylamine
Routes of
administration
Oral[1]
Drug classSerotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Pharmacokinetic data
Duration of action~8 hours[1]
Identifiers
  • 1-(4-bromo-2,5-dimethoxyphenyl)butan-2-amine
CAS Number
PubChemCID
ChemSpider
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC12H18BrNO2
Molar mass288.185 g·mol−1
3D model (JSmol)
Melting point204 to 206 °C (399 to 403 °F)
  • CCC(CC1=CC(=C(C=C1OC)Br)OC)N
  • InChI=1S/C12H18BrNO2/c1-4-9(14)5-8-6-12(16-3)10(13)7-11(8)15-2/h6-7,9H,4-5,14H2,1-3H3
  • Key:QQPRORAZQWLMTQ-UHFFFAOYSA-N

4C-B, also known as4C-DOB orDOB-B, as well as4-bromo-2,5-dimethoxy-α-ethylphenethylamine, is a lesser-knownpsychedelic drug of thephenethylamine,phenylisobutylamine, and4C families related to2C-B (the2Canalogue) andDOB (theDOx analogue).[2] It is a reasonably potent5-HT2A receptorpartial agonist with a Ki of 7.6 nM, but has relatively low efficacy (15% relative to 5-HT).[3] It is briefly mentioned inAlexander Shulgin's 1991 bookPiHKAL (Phenethylamines I Have Known And Loved), but was never tested by Shulgin.[4] Subsequently, the drug was tested byDaniel Trachsel and colleagues, and was found to be active in a dose range of 50 to 80 mg with aduration of around 8 hours.[1] It produced pronounced psychedelic effects, though with generally milder effects than 2C-B or DOB.[1]

See also

[edit]

References

[edit]
  1. ^abcdTrachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: Von der Struktur zur Funktion. Nachtschatten Verlag AG. p. 832.ISBN 978-3-03788-700-4.Das α-Ethylhomologon von 2C-B (6) trägt den Namen (303; auch 4C-B) und wurde von Rausch eingehender untersucht [140, 145]. Es vermochte eine ausgeprägte psychedelische Wirkung mit Bewusstseinsvertiefung, Euphorie und Sensationen besonders im Bereich des Tastsinns hervorzurufen (50—80mg, rund acht Stunden Wirkdauer). Visuelle Pseudohalluzinationen traten kaum auf. Das Iodoanalogon DOI-B (304) wurde nur bis zu einer Dosierung von 4mg geprüft und zeigte dabei keinerlei Wirkungen [8].
  2. ^Standridge RT, Howell HG, Tilson HA, Chamberlain JH, Holava HM, Gylys JA, Partyka RA, Shulgin AT (February 1980). "Phenylalkylamines with potential psychotherapeutic utility. 2. Nuclear substituted 2-amino-1-phenylbutanes".Journal of Medicinal Chemistry.23 (2):154–62.doi:10.1021/jm00176a010.PMID 7359529.
  3. ^Glennon RA, Bondarev ML, Khorana N, Young R, May JA, Hellberg MR, McLaughlin MA, Sharif NA (November 2004). "Beta-oxygenated analogues of the 5-HT2A serotonin receptor agonist 1-(4-bromo-2,5-dimethoxyphenyl)-2-aminopropane".Journal of Medicinal Chemistry.47 (24):6034–41.doi:10.1021/jm040082s.PMID 15537358.
  4. ^Shulgin A,Shulgin A (September 1991).PiHKAL: A Chemical Love Story.Berkeley, California:Transform Press.ISBN 0-9630096-0-5.OCLC 25627628.

External links

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