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Dimemebfe

From Wikipedia, the free encyclopedia
Psychedelic drug
Pharmaceutical compound
Dimemebfe
Clinical data
Other names5-Methoxy-N,N-dimethyl-3-(2-aminoethyl)benzofuran;N,N-Dimethyl-5-methoxy-benzofuranylethylamine; 5-MeO-BFE; 5-MeO-DMBF; 1-Oxa-5-MeO-DMT; O-5-MeO-DMT; "Head f--k"; "Head fuck"
Drug classSerotonin receptor modulator;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Legal status
Legal status
Identifiers
  • 2-(5-Methoxy-1-benzofuran-3-yl)-N,N-dimethylethanamine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H17NO2
Molar mass219.284 g·mol−1
3D model (JSmol)
  • CN(C)CCc1coc(c1c2)ccc2OC
  • InChI=1S/C13H17NO2/c1-14(2)7-6-10-9-16-13-5-4-11(15-3)8-12(10)13/h4-5,8-9H,6-7H2,1-3H3 ☒N
  • Key:WBPQJTBOQCCTFX-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Dimemebfe, also known as 5-methoxy-N,N-dimethyl-3-(2-aminoethyl)benzofuran (5-MeO-BFE or5-MeO-DMBF) or as1-oxa-5-MeO-DMT, is apsychedelic drug of thebenzofuran family related to the psychedelictryptamine5-MeO-DMT.[1][2][3][4] It is theanalogue andbioisostere of 5-MeO-DMT in which thenitrogenatom of theindolering has been replaced with anoxygen atom, making dimemebfe a benzofuran rather than tryptamine derivative.[1][2][3][4] The drug has been encountered as a noveldesigner drug.[3]

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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Dimemebfe acts as anagonist of theserotonin5-HT1A and5-HT2 family ofserotoninreceptors.[4] It is several times lesspotent as aserotonin receptor agonist than5-MeO-DMT and with relatively more activity at the serotonin 5-HT1A receptor, but still shows strongest actions at the 5-HT2 family of receptors.[4]

Chemistry

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Synthesis

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Thechemical synthesis of dimemembfe has been described.[4]

Analogues

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Analogues of dimemebfe include thebenzofurans5-MeO-DiBF (1-oxa-5-MeO-DiPT),3-APB (1-oxa-AMT), andmebfap (5-MeO-3-APB; 1-oxa-5-MeO-AMT), thebenzothiopheneS-DMT (1-thia-DMT), and thetryptamine5-MeO-DMT, among others.

History

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Dimemebfe was first described in thescientific literature byDavid E. Nichols and colleagues in 1992.[3][4] Subsequently, it emerged as a noveldesigner drug by 2012.[3]

Society and culture

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Legal status

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Canada

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Dimemebfe is not acontrolled substance inCanada as of 2025.[5]

United States

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Dimemebfe is not an explicitlycontrolled substance in theUnited States.[6] However, it could be considered acontrolled substance under theFederal Analogue Act if intended for human consumption.

Dimemebfe is aSchedule Icontrolled substance in theUnited States state ofAlabama.[7]

See also

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References

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  1. ^abNichols, David E. (2012)."Structure–activity relationships of serotonin 5‐HT 2A agonists".Wiley Interdisciplinary Reviews: Membrane Transport and Signaling.1 (5):559–579.doi:10.1002/wmts.42.ISSN 2190-460X. Retrieved7 January 2026.
  2. ^abNichols DE (2018). "Chemistry and Structure-Activity Relationships of Psychedelics".Curr Top Behav Neurosci.36:1–43.doi:10.1007/7854_2017_475.PMID 28401524.
  3. ^abcdeCasale JF, Hays PA (2012)."The Characterization of 2-(5-Methoxy-1-benzofuran-3-yl)-N,N-dimethylethanamine (5-MeO-BFE) and Differentiation from its N-Ethyl Analog"(PDF).Microgram Journal.9 (1):39–45. Archived fromthe original(PDF) on 2017-05-13. Retrieved2015-02-23.
  4. ^abcdefTomaszewski Z, Johnson MP, Huang X, Nichols DE (May 1992). "Benzofuran bioisosteres of hallucinogenic tryptamines".Journal of Medicinal Chemistry.35 (11):2061–2064.doi:10.1021/jm00089a017.PMID 1534585.
  5. ^"Controlled Drugs and Substances Act".Department of Justice Canada. Retrieved19 January 2026.
  6. ^Orange Book: List of Controlled Substances and Regulated Chemicals (January 2026)(PDF),United States: U.S.Department of Justice:Drug Enforcement Administration (DEA): Diversion Control Division, January 2026
  7. ^"Alabama Senate Bill 333 - Controlled substances, Schedule I, additional synthetic controlled substances and analogue substances included in, trafficking in controlled substance analogues, requisite weight increased, Secs. 13A-12-231, 20-2-23 am'd". March 2014. Retrieved28 September 2015.

External links

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