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2CB-Ind

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
2CB-Ind
Clinical data
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • (5-bromo-4,7-dimethoxy-2,3-dihydro-1H-inden-1-yl)methanamine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC12H16BrNO2
Molar mass286.169 g·mol−1
3D model (JSmol)
  • COc1c(Br)cc(OC)c2c1CCC2CN
  • InChI=1S/C12H16BrNO2/c1-15-10-5-9(13)12(16-2)8-4-3-7(6-14)11(8)10/h5,7H,3-4,6,14H2,1-2H3 checkY
  • Key:HCLPGYNQMVSQIM-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

2CB-Ind is aconformationally-restrictedderivative of thephenethylaminehallucinogen2C-B which was developed byDavid E. Nichols and colleagues. It acts as a moderately potent and selectiveagonist for the5-HT2A and5-HT2Creceptors, but unlike the corresponding benzocyclobutene derivativeTCB-2 which is considerably more potent than the parent compound2C-B, 2CB-Ind is several times weaker, withracemic 2CB-Ind having aKi of 47nM at the human 5-HT2A receptor, only slightly more potent than themescaline analogue (R)-jimscaline.[1][2]

See also

[edit]

References

[edit]
  1. ^McLean TH, Parrish JC, Braden MR, Marona-Lewicka D, Gallardo-Godoy A, Nichols DE (September 2006). "1-Aminomethylbenzocycloalkanes: conformationally restricted hallucinogenic phenethylamine analogues as functionally selective 5-HT2A receptor agonists".Journal of Medicinal Chemistry.49 (19):5794–803.CiteSeerX 10.1.1.688.9849.doi:10.1021/jm060656o.PMID 16970404.
  2. ^Braden MR (2007).Towards a biophysical understanding of hallucinogen action (PhD.). Purdue University.ProQuest 304838368.
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
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Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
Others
Cyclized
Lysergamides
  • Bioisosteres:JRT
Others
Natural sources
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
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5-HT5A
5-HT6
5-HT7
Phenethylamines
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(and further-extended)
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(and close relatives)
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(phenidates)
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(phenmetrazines)
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(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
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