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5-MeO-DiBF

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
5-MeO-DiBF
Clinical data
Routes of
administration
?
ATC code
  • None
Legal status
Legal status
Identifiers
  • N-[2-(5-methoxy-1-benzofuran-3-yl)ethyl]-N-(propan-2-yl)propan-2-amine
CAS Number
  • none
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC17H25NO2
Molar mass275.392 g·mol−1
3D model (JSmol)
  • COC1=CC=C(OC=C2CCN(C(C)C)C(C)C)C2=C1
  • InChI=1S/C17H25NO2/c1-12(2)18(13(3)4)9-8-14-11-20-17-7-6-15(19-5)10-16(14)17/h6-7,10-13H,8-9H2,1-5H3
  • Key:NBFMSQBTYHYVKP-UHFFFAOYSA-N

5-MeO-DiBF is apsychedelic[1] that has been sold online as adesigner drug and was first definitively identified in December 2015 by a forensic laboratory inSlovenia.[2] It is thought to act as anagonist for the5-HT1A and5-HT2 family ofserotoninreceptors. It is related in structure to thepsychedelictryptamine derivative5-MeO-DiPT, but with theindolenitrogen replaced by oxygen, making 5-MeO-DiBF abenzofuran derivative. It is several times less potent as a serotonin agonist than 5-MeO-DiPT and with relatively more activity at 5-HT1A, but still shows strongest effects at the 5-HT2 family of receptors.[3][4]

Legal status

[edit]

5-MeO-DiBF is not controlled under the1971 Convention on Psychotropic Substances, so thus it has a legal grey area in manycountries, but it's possible it could be illegal under so-called analogue acts if sold for human consumption.

See also

[edit]

References

[edit]
  1. ^Casale JF, Hays PA."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.
  2. ^"Europol 2015 Annual Report on the implementation of Council Decision 2005/387/JHA"(PDF). European Monitoring Center for Drugs and Drug Addiction.
  3. ^Tomaszewski Z, Johnson MP, Huang X, Nichols DE (May 1992). "Benzofuran bioisosteres of hallucinogenic tryptamines".Journal of Medicinal Chemistry.35 (11):2061–4.doi:10.1021/jm00089a017.PMID 1534585.
  4. ^McKenna DJ, Repke DB, Lo L, Peroutka SJ (March 1990)."Differential interactions of indolealkylamines with 5-hydroxytryptamine receptor subtypes".Neuropharmacology.29 (3):193–8.doi:10.1016/0028-3908(90)90001-8.PMID 2139186.S2CID 24188017.
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
Retrieved from "https://en.wikipedia.org/w/index.php?title=5-MeO-DiBF&oldid=1322774079"
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