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2-Bromomescaline

From Wikipedia, the free encyclopedia
Mescaline derivative drug
Not to be confused with2C-B (sometimes also referred to as "bromomescaline")

Pharmaceutical compound
2-Bromomescaline
Clinical data
ATC code
  • None
Identifiers
  • 2-(2-Bromo-3,4,5-trimethoxyphenyl)ethanamine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC11H16BrNO3
Molar mass290.157 g·mol−1
3D model (JSmol)
  • COC1=C(C(=C(C(=C1)CCN)Br)OC)OC
  • InChI=1S/C11H16BrNO3/c1-14-8-6-7(4-5-13)9(12)11(16-3)10(8)15-2/h6H,4-5,13H2,1-3H3
  • Key:UXQBKANLBLUVMK-UHFFFAOYSA-N

2-Bromomescaline (2-Br-M) is aderivative of thephenethylaminehallucinogenmescaline which has an unusual 2-bromo substitution.[1][2] It is anagonist forserotonin receptors, with abinding affinity of 215 nM at5-HT1A, 513 nM at5-HT2A and 379 nM at5-HT2C, so while it is around 10 times more tightly binding than mescaline at 5-HT1A and 5-HT2A receptors, it is over 20 times more potent at 5-HT2C.[3] It has been reported as adesigner drug, first identified in Austria in January 2023.[4]

See also

[edit]

References

[edit]
  1. ^Shulgin A, Manning T, Daley PF (2011).The Shulgin Index. Volume 1. Psychedelic Phenethylamines and Related Compounds. Transform Press. pp. 280–281, 355.ISBN 978-0-9630096-3-0.
  2. ^Pecherer B, Sunbury RC, Brossi A (June 1972). "A novel synthesis of aromatic methoxy and methylenedioxy substituted 2,3,4,5-tetrahydro-1H3-benzazepines".Journal of Heterocyclic Chemistry.9 (3):609–616.doi:10.1002/jhet.5570090322.
  3. ^Trachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine Von der Struktur zur Funktion. Nachtschatten Verlag AG. pp. 908–910.ISBN 978-3-03788-700-4.
  4. ^"New psychoactive substances - the current situation in Europe"(PDF).European Drug Report. European Union Drugs Agency (EUDA). 2024.
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