Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

5-MBPB

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
5-MBPB
Clinical data
ATC code
  • none
Legal status
Legal status
Identifiers
  • 1-(1-benzofuran-5-yl)-N-methylbutan-2-amine
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H17NO
Molar mass203.28 g/mol (freebase) 239.78 g/mol (hydrochloride) g·mol−1
3D model (JSmol)
  • CCC(CC1=CC2=C(OC=C2)C=C1)NC
  • InChI=1S/C13H17NO/c1-3-12(14-2)9-10-4-5-13-11(8-10)6-7-15-13/h4-8,12,14H,3,9H2,1-2H3
  • Key:CTEZPBCLIKEASW-UHFFFAOYSA-N

5-MBPB (also known as5-MPBP and5-MABB) is anamphetamine andphenylisobutylaminederivative which isstructurally related toMDMA and has been sold as adesigner drug. It can be described as thebenzofuran-5-ylanalogue ofMBDB or the butanaminehomologue of5-MAPB, and is also astructural isomer of5-EAPB and6-EAPB. Anecdotal reports suggest this compound has been sold as a designer drug in various European countries since early 2015, but the first definitive identification was made in December 2015 by a forensic laboratory inSlovenia.[1]

5-MBPB is similar in structure to compounds such as5-APB which are claimed to be agonists of the5-HT2C receptor.[2]

5-MBPB (5-MABB) has been found to act as apotentserotonin–norepinephrine–dopamine releasing agent (SNDRA), with preference for induction ofserotonin release overnorepinephrine anddopamine release, and fully substitutes for MDMA in animaldrug discrimination tests.[3] Unlike5-MAPB, it is a relatively weakserotonin5-HT1B receptoragonist.[4]

See also

[edit]

References

[edit]
  1. ^European Monitoring Center for Drugs and Drug Addiction – Europol 2015 Annual Report on the implementation of Council Decision 2005/387/JHA
  2. ^US patent 7045545, Karin Briner et al, "Aminoalkylbenzofurans as serotonin (5-HT(2c)) agonists", published 2000-01-19, issued 2006-16-03 
  3. ^Johnson CB, Walther D, Baggott MJ, Baker LE, Baumann MH (September 2024)."Novel Benzofuran Derivatives Induce Monoamine Release and Substitute for the Discriminative Stimulus Effects of 3,4-Methylenedioxymethamphetamine".J Pharmacol Exp Ther.391 (1):22–29.doi:10.1124/jpet.123.001837.PMC 11413916.PMID 38272669.
  4. ^US 20230150963, Matthew Baggott, "Advantageous benzofuran compositions for mental disorders or enhancement", published 2023 May 18, assigned toTactogen 

External links

[edit]
Phenethylamines
Non-ring-extended
Benzodioxoles
(methylenedioxy- or MDxx)
Benzodioxines
(ethylenedioxy-)
Benzofurans
Dihydrobenzofurans
Benzothiophenes
Benzothiazoles
Benzoxathioles
Indanes
Indoles
Naphthalenes
Tetralins
Others
Cyclized
phenethylamines
2-Aminoindanes
1-Aminomethylindanes
2-Aminotetralins
Aminorexes
Tryptamines
α-Alkyltryptamines
Others
Benzofurans
Benzothiophenes
Indolizines
Isotryptamines
Others
DRAsTooltip Dopamine releasing agents
NRAsTooltip Norepinephrine releasing agents
SRAsTooltip Serotonin releasing agents
Others
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
Retrieved from "https://en.wikipedia.org/w/index.php?title=5-MBPB&oldid=1322835628"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp