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2CBFly-NBOMe

From WikiProjectMed
2CBFly-NBOMe
Kekulé, skeletal formula of 2CBFly-NBOMe
Kekulé, skeletal formula of 2CBFly-NBOMe
Names
Preferred IUPAC name
2-(8-Bromo-2,3,6,7-tetrahydrobenzo[1,2-b:4,5-b′]difuran-4-yl)-N-[(2-methoxyphenyl)methyl]ethan-1-amine
Identifiers
3D model (JSmol)
Abbreviations2CBFly-NBOMe
ChemSpider
  • InChI=1S/C20H22BrNO3/c1-23-17-5-3-2-4-13(17)12-22-9-6-14-15-7-10-25-20(15)18(21)16-8-11-24-19(14)16/h2-5,22H,6-12H2,1H3 checkY
    Key: CUFCITSPWAZWHS-UHFFFAOYSA-N checkY
  • COc1ccccc1CNCCc1c2CCOc2c(Br)c2CCOc12
  • COC1=C(CNCCC2=C3OCCC3=C(Br)C3=C2CCO3)C=CC=C1
Properties
C20H22BrNO3
Molar mass404.298 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

2CBFly-NBOMe (NBOMe-2C-B-FLY,Cimbi-31) is adrug of thephenethylamine,DOx, andFLY families. It was indirectly derived from thephenethylaminehallucinogen2C-B, and related to benzodifurans like2C-B-FLY andN-benzylphenethylamines like25I-NBOMe. It was discovered in 2002,[1] and further researched by Ralf Heim at theFree University of Berlin,[2] and subsequently investigated in more detail by a team atPurdue University led byDavid E. Nichols.[3] It acts as a potentpartial agonist for the5-HT2Aserotoninreceptor subtype.[4][5][6]

Analogues and derivatives

Legality

United Kingdom

This substance is aClass A drug in the United Kingdom as a result of theN-benzylphenethylamine catch-all clause in theMisuse of Drugs Act 1971.[11]

United States

2CBFly-NBOMe is a controlled substance in Vermont as of January 2016.[12]

References

  1. Elz S, Klass T, Heim R, Warnke U, Pertz HH (2002). "Development of highly potent partial agonists and chiral antagonists as tools for the study of 5-HT2A-receptor mediated function".Naunyn-Schmiedeberg's Archives of Pharmacology.365 (1 Suppl):R21 –R40.doi:10.1007/s00210-002-0604-4.
  2. Heim R (2004).Synthese und Pharmakologie potenter 5-HT2A-Rezeptoragonisten mit N-2-Methoxybenzyl-Partialstruktur. Entwicklung eines neuen Struktur-Wirkungskonzepts (PhD.). Free University of Berlin.
  3. Braden MR (2007).Towards a biophysical understanding of hallucinogen action (PhD.). Purdue University.ProQuest 304838368.
  4. Silva ME, Heim R, Strasser A, Elz S, Dove S (January 2011). "Theoretical studies on the interaction of partial agonists with the 5-HT2A receptor".Journal of Computer-Aided Molecular Design.25 (1):51–66.Bibcode:2011JCAMD..25...51S.CiteSeerX 10.1.1.688.2670.doi:10.1007/s10822-010-9400-2.PMID 21088982.S2CID 3103050.
  5. Ettrup A, Hansen M, Santini MA, Paine J, Gillings N, Palner M, et al. (April 2011). "Radiosynthesis and in vivo evaluation of a series of substituted 11C-phenethylamines as 5-HT (2A) agonist PET tracers".European Journal of Nuclear Medicine and Molecular Imaging.38 (4):681–93.doi:10.1007/s00259-010-1686-8.PMID 21174090.S2CID 12467684.
  6. Hansen M (2011).Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain (PhD.). University of Copenhagen. Archived fromthe original on 2013-10-22. Retrieved2012-11-02.
  7. "Explore N-(2C-B)-Fentanyl | PiHKAL · info".isomerdesign.com.
  8. "Explore N-(2C-FLY)-Fentanyl | PiHKAL · info".isomerdesign.com.
  9. Glennon, Richard A.; Bondarev, Mikhail L.; Khorana, Nantaka; Young, Richard; May, Jesse A.; Hellberg, Mark R.; McLaughlin, Marsha A.; Sharif, Najam A. (November 2004). "β-Oxygenated Analogues of the 5-HT2ASerotonin Receptor Agonist 1-(4-Bromo-2,5-dimethoxyphenyl)-2-aminopropane".Journal of Medicinal Chemistry.47 (24):6034–6041.doi:10.1021/jm040082s.ISSN 0022-2623.PMID 15537358.
  10. Beta-hydroxyphenylalkylamines and their use for treating glaucoma
  11. "The Misuse of Drugs Act 1971 (Ketamine etc.) (Amendment) Order 2014".UK Statutory Instruments 2014 No. 1106. www.legislation.gov.uk.
  12. "Regulated Drugs Rule"(PDF). Vermont Department of Health. Archived fromthe original(PDF) on 5 June 2016. Retrieved14 October 2015.
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
Others
Cyclized
Lysergamides
  • Bioisosteres:JRT
Others
Natural sources
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
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
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