6-MBPB

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6-MBPB
File:6MBPB structure.png
Clinical data
Other names6-MABB; 6-(2-Methylaminobutyl)benzofuran
Drug classSerotonin–norepinephrine–dopamine releasing agent; Entactogen
Identifiers
  • 1-(1-benzofuran-6-yl)-N-methylbutan-2-amine
PubChem CID
ChemSpider
ChEMBL
E number{{#property:P628}}
CompTox Dashboard (EPA)
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Chemical and physical data
FormulaC13H17NO
Molar mass203.285 g·mol−1
3D model (JSmol)
  • CCC(CC1=CC2=C(C=C1)C=CO2)NC
  • InChI=1S/C13H17NO/c1-3-12(14-2)8-10-4-5-11-6-7-15-13(11)9-10/h4-7,9,12,14H,3,8H2,1-2H3
  • Key:LVDZDORQOMAGGH-UHFFFAOYSA-N

6-MBPB, also known as 6-(2-methylaminobutyl)benzofuran (6-MABB), is a monoamine releasing agent (MRA) and entactogen-like drug of the amphetamine, phenylisobutylamine, and benzofuran families.[1][2][3][4][5] It is a positional isomer of 5-MBPB (5-MABB).[1][2][3][4][5]

The drug appears to act as a serotonin–norepinephrine–dopamine releasing agent (SNDRA).[1][2] The EC50Tooltip half-maximal effective concentration values for induction of monoamine release in rat brain synaptosomes have been reported for the individual enantiomers of 6-MBPB.[2] In the case of (S)-6-MBPB, they were 54 nM for serotonin, 77 nM for norepinephrine, and 41 nM for dopamine, whereas for (R)-6-MBPB, they were 172 nM for serotonin, 227 nM for norepinephrine, and inactive for dopamine.[2] Hence, (S)-6-MBPB is an SNDRA, whereas (R)-MBPB is a serotonin–norepinephrine releasing agent (SNRA).[2] The enantiomers showed a mixed profile of acting as full versus partial releasers.[2] Unlike 5-MAPB, it is a relatively weak serotonin 5-HT1B receptor agonist.[6] 6-MBPB partially substituted for MDMA in animal drug discrimination tests at lower doses and fully substituted for MDMA at the highest dose, suggesting that it has entactogen-like effects.[1][2][4]

Along with 5-MBPB, 6-MBPB was patented by Matthew Baggott and Tactogen in 2021.[5] It was first described in the scientific literature by 2022.[3][4] 6-MBPB, along with other drugs like 5-MBPB, is being investigated as a novel MDMA-like drug for potential therapeutic purposes in medicine.[1][2]

See also

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References

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  1. ^ a b c d e Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  2. ^ a b c d e f g h i Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
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  5. ^ a b c Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  6. ^ US 20230150963, Matthew Baggott, "Advantageous benzofuran compositions for mental disorders or enhancement", published Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value)., assigned to Tactogen 
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