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5-MeO-NBpBrT

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
5-MeO-NBpBrT
Identifiers
  • N-(4-Bromobenzyl)-2-(5-methoxy-1H-indol-3-yl)ethanamine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H19BrN2O
Molar mass359.267 g·mol−1
3D model (JSmol)
  • BrC1=CC=C(CNCCC2=CNC3=CC=C(OC)C=C23)C=C1
  • InChI=1S/C18H19BrN2O/c1-22-16-6-7-18-17(10-16)14(12-21-18)8-9-20-11-13-2-4-15(19)5-3-13/h2-7,10,12,20-21H,8-9,11H2,1H3 checkY
  • Key:XHLOUFPZLUULGI-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

5-MeO-NBpBrT (5-Methoxy-N-(4-bromobenzyl)tryptamine) is a N-substituted member of themethoxytryptamine family of compounds. Like other such compounds it acts as anantagonist for the5-HT2Areceptor, with a claimed 100x selectivity over the closely related5-HT2C receptor.[1] While N-benzyl substitution of psychedelic phenethylamines often results in potent 5-HT2A agonists, it had been thought that N-benzyl tryptamines show much lower efficacy and are either very weakpartial agonists or antagonists at 5-HT2A,[2][3] though more recent research has shown stronger agonist activity for 3-substituted benzyl derivatives.[4] Extending the benzyl group to a substituted phenethyl can also recover agonist activity in certain cases.[5]

See also

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References

[edit]
  1. ^Glennon RA, Dukat M, el-Bermawy M, Law H, De los Angeles J, Teitler M, et al. (June 1994). "Influence of amine substituents on 5-HT2A versus 5-HT2C binding of phenylalkyl- and indolylalkylamines".Journal of Medicinal Chemistry.37 (13):1929–35.doi:10.1021/jm00039a004.PMID 8027974.
  2. ^Silva M (2009).Theoretical study of the interaction of agonists with the 5-HT2A receptor (PhD thesis). Universität Regensburg.
  3. ^Silva ME, Heim R, Strasser A, Elz S, Dove S (January 2011). "Theoretical studies on the interaction of partial agonists with the 5-HT2A receptor".Journal of Computer-Aided Molecular Design.25 (1):51–66.Bibcode:2011JCAMD..25...51S.CiteSeerX 10.1.1.688.2670.doi:10.1007/s10822-010-9400-2.PMID 21088982.S2CID 3103050.
  4. ^Nichols DE, Sassano MF, Halberstadt AL, Klein LM, Brandt SD, Elliott SP, Fiedler WJ (July 2015)."N-Benzyl-5-methoxytryptamines as Potent Serotonin 5-HT2 Receptor Family Agonists and Comparison with a Series of Phenethylamine Analogues".ACS Chemical Neuroscience.6 (7):1165–75.doi:10.1021/cn500292d.PMC 4505863.PMID 25547199.
  5. ^Jensen N (2004).Tryptamines as Ligands and Modulators of the Serotonin 5-HT2A Receptor and the Isolation of Aeruginascin from the Hallucinogenic Mushroom Inocybe aeruginascens(PDF) (PhD thesis). Georg-August-Universität zu Göttingen.
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
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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