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2CBCB-NBOMe

From Wikipedia, the free encyclopedia

Chemical compound
Pharmaceutical compound
2CBCB-NBOMe
Clinical data
Other namesNBOMe-2CBCB; NBOMe-TCB-2; TCB-2-NBOMe
Drug classSerotonin receptor modulator;Serotonin 5-HT2A receptor agonist
Legal status
Legal status
Identifiers
  • 1-(3-bromo-2,5-dimethoxy-7-bicyclo[4.2.0]octa-1(6),2,4-trienyl)-N-[(2-methoxyphenyl)methyl]methanamine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC19H22BrNO3
Molar mass392.293 g·mol−1
3D model (JSmol)
  • COC1=CC=CC=C1CNCC2CC3=C2C(=CC(=C3OC)Br)OC
  • InChI=1S/C19H22BrNO3/c1-22-16-7-5-4-6-12(16)10-21-11-13-8-14-18(13)17(23-2)9-15(20)19(14)24-3/h4-7,9,13,21H,8,10-11H2,1-3H3 checkY
  • Key:CLSBQRBXTFTLEX-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

2CBCB-NBOMe, orNBOMe-TCB-2, is aserotonin receptor modulator andcyclized phenethylamine.[1][2] It is theNBOMederivative of thepsychedelic drugTCB-2 (2C-BCB).[1][2]

Interactions

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See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Pharmacology

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Pharmacodynamics

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2CBCB-NBOMe acts as apotent andselectiveagonist of theserotonin5-HT2A and5-HT2C receptors, with anaffinity (Ki) of 0.27 nM at the human serotonin 5-HT2A receptor, similar to that of other drugs such asTCB-2,25I-NBOMe, andBromo-DragonFLY.[1][2]

History

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2CB2CB-NBOMe was first described in thescientific literature by the lab ofDavid E. Nichols and colleagues in 2007.[1][2] It was part of an ongoing research program focused on mapping of the specific amino acid residues responsible for ligand binding to theserotonin5-HT2Areceptor.[1][2]

Society and culture

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Legal status

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Canada

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2CBCB-NBOMe is not acontrolled substance inCanada as of 2025.[3]

United Kingdom

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This substance is aClass A drug in theUnited Kingdom as a result of theN-benzylphenethylamine catch-all clause in theMisuse of Drugs Act 1971.[4]

United States

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2CBCB-NBOMe is a controlled substance in Vermont as of January 2016.[5]

See also

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References

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  1. ^abcdeTrachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German) (1st ed.). Solothurn: Nachtschatten-Verlag. p. 861.ISBN 978-3-03788-700-4.OCLC 858805226. Archived fromthe original on 21 August 2025.
  2. ^abcdeBraden MR (2007).Towards a biophysical understanding of hallucinogen action (Ph.D.). Purdue University.ProQuest 304838368.
  3. ^"Controlled Drugs and Substances Act".Department of Justice Canada. Retrieved19 January 2026.
  4. ^"The Misuse of Drugs Act 1971 (Ketamine etc.) (Amendment) Order 2014".UK Statutory Instruments 2014 No. 1106. www.legislation.gov.uk.
  5. ^"Regulated Drugs Rule"(PDF). Vermont Department of Health. Archived fromthe original(PDF) on 23 January 2014. Retrieved14 October 2015.

External links

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