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25b-nboh

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Title: 25b-nboh  
Author: World Heritage Encyclopedia
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Subject: 25C-NBOH, 25CN-NBOH, 25I-NBOH, 25B-NBOMe, 25I-NBOMe
Collection: Designer Drugs, Organobromides, Psychedelic Phenethylamines
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25b-nboh

25B-NBOH
Systematic (IUPAC) name
2-((4-bromo-2,5-dimethoxyphenethylamino)methyl)phenol
Clinical data
Legal status
Identifiers
CAS Registry Number
Chemical data
Formula C17H20BrNO3
Molecular mass 365,06 g/mol

25B-NBOH (2C-B-NBOH, NBOH-2C-B) is a derivative of the phenethylamine derived hallucinogen 2C-B which has been sold as a designer drug. It has similar serotonin receptor affinity to the better-known compound 25B-NBOMe.[1][2][3][4][5][6]

See also

References

  1. ^ Heim, Ralf (19 March 2004). -Rezeptoragonisten mit N-2-Methoxybenzyl-Partialstruktur"2A"Synthese und Pharmakologie potenter 5-HT. Freie Unversität Berlin. Retrieved 27 June 2015. 
  2. ^ Hansen, M.; Phonekeo, K.; Paine, J. S.; Leth-Petersen, S.; Begtrup, M.; Bräuner-Osborne, H.; Kristensen, J. L. (2014). Agonists"2A/2C"Synthesis and Structure-Activity Relationships of N-Benzyl Phenethylamines as 5-HT. ACS Chemical Neuroscience 5 (3): 243–9.  
  3. ^ Martin Hansen (2011). "Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain." (PDF). University of Copenhagen. Retrieved 27 June 2015. 
  4. ^ Ettrup, A.; Hansen, M.; Santini, M. A.; Paine, J.; Gillings, N.; Palner, M.; Lehel, S.; Herth, M. M.; Madsen, J. (2010). "Radiosynthesis and in vivo evaluation of a series of substituted 11C-phenethylamines as 5-HT2A agonist PET tracers". European Journal of Nuclear Medicine and Molecular Imaging 38 (4): 681–693.  
  5. ^ Silva, M. E.; Heim, R.; Strasser, A.; Elz, S.; Dove, S. (2011). "Theoretical studies on the interaction of partial agonists with the 5-HT2A receptor". Journal of Computer-aided Molecular Design 25 (1): 51–66.  
  6. ^ Braden, M. R.; Parrish, J. C.; Naylor, J. C.; Nichols, D. E. (2006). with superpotent N-benzyl phenethylamine agonists"6.52340 and Phe6.51339"Molecular interaction of serotonin 5-HT2A receptor residues Phe. Molecular Pharmacology 70 (6): 1956–1964.  


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