Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

2CJP

From Wikipedia, the free encyclopedia
Pharmaceutical compound
2CJP
Clinical data
ATC code
  • None
Identifiers
  • 4-(4-bromo-2,5-dimethoxyphenyl)-2,3,4,5-tetrahydro-1H-2-benzazepine
Chemical and physical data
FormulaC18H20BrNO2
Molar mass362.267 g·mol−1
3D model (JSmol)
  • COc1cc(Br)c(cc1C1CNCc2c(C1)cccc2)OC
  • InChI=1S/C18H20BrNO2/c1-21-17-9-16(19)18(22-2)8-15(17)14-7-12-5-3-4-6-13(12)10-20-11-14/h3-6,8-9,14,20H,7,10-11H2,1-2H3
  • Key:FQAXYSXGRJQKMV-UHFFFAOYSA-N

2CJP, also known as4-(4-bromo-2,5-dimethoxyphenyl)-2,3,4,5-tetrahydro-1H-2-benzazepine, is aserotonin receptor modulator of thephenethylamine,2C, andN-benzylphenethylamine families.[1][2][3][4] It is acyclized phenethylamineanalogue of25B-NBOMe in which theN-benzylethylamineside chain has beencyclized to form atetrahydrobenzazepinering.[1][2] The drug showsaffinity for theserotonin5-HT2A and5-HT2C receptors (Ki = 19–457 nM and 227–3,240 nM, respectively).[3][4] 2CJP was first described in thescientific literature by Michael Robert Braden of the lab ofDavid E. Nichols atPurdue University in 2007.[1][2]

See also

[edit]

References

[edit]
  1. ^abcTrachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German) (1 ed.). Solothurn: Nachtschatten-Verlag. pp. 837–840,866–867.ISBN 978-3-03788-700-4.OCLC 858805226.
  2. ^abcBraden MR (2007).Towards a Biophysical Understanding of Hallucinogen Action (Ph.D. thesis). Purdue University.ProQuest 304838368. Archived from the original on 2025-01-21. Retrieved2025-08-01.{{cite thesis}}: CS1 maint: bot: original URL status unknown (link)
  3. ^abHansen M (2010-12-16).Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain (Ph.D. thesis). University of Copenhagen.doi:10.13140/RG.2.2.33671.14245.
  4. ^abJuncosa JI, Hansen M, Bonner LA, Cueva JP, Maglathlin R, McCorvy JD, Marona-Lewicka D, Lill MA, Nichols DE (January 2013)."Extensive rigid analogue design maps the binding conformation of potent N-benzylphenethylamine 5-HT2A serotonin receptor agonist ligands".ACS Chemical Neuroscience.4 (1):96–109.doi:10.1021/cn3000668.PMC 3547484.PMID 23336049.

External links

[edit]
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
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
Stub icon

Thisdrug article relating to thenervous system is astub. You can help Wikipedia byadding missing information.

Retrieved from "https://en.wikipedia.org/w/index.php?title=2CJP&oldid=1332782482"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2026 Movatter.jp