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2CBFly-NBOMe

From Wikipedia, the free encyclopedia
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

[edit]

Analogues and derivatives of2C-B:

25-N:

25-NB:

25-NM:

Substituted benzofurans:

N-(2C)-fentanyl:

Other:

Legality

[edit]

United Kingdom

[edit]

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

[edit]

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

References

[edit]
  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
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Cathinones
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(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
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(phenmetrazines)
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(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
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