Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

TFMBOX

From Wikipedia, the free encyclopedia

Not to be confused withBOx (psychedelics).
Pharmaceutical compound
TFMBOX
Clinical data
Other names"Compound 5c"
Drug classSerotonin receptor modulator;Serotonergic psychedelic;Hallucinogen
Identifiers
  • 7-methoxy-8-(trifluoromethyl)-2,3,4,5-tetrahydro-1-benzoxepin-4-amine
CAS Number
Chemical and physical data
FormulaC12H14F3NO2
Molar mass261.244 g·mol−1
3D model (JSmol)
  • COc1cc2CC(N)CCOc2cc1C(F)(F)F
  • InChI=1S/C12H14F3NO2/c1-17-11-5-7-4-8(16)2-3-18-10(7)6-9(11)12(13,14)15/h5-6,8H,2-4,16H2,1H3
  • Key:NAOXZRLWFAOHAP-UHFFFAOYSA-N

TFMBOX is a putativeserotonergic psychedelic of thephenethylamine andbenzoxepin ("BOX") families.[1][2][3] It is thecyclized phenethylamineanalogue ofDOTFM and2C-TFM in which theα carbon has been connected to the 2-methoxy group via anethylchain to form a benzoxepinring system.[1][2]

The drug was assessed at and showedaffinity for theserotonin5-HT2A and5-HT1A receptors, with Ki values of 340 nM and 1,300 nM, respectively.[2] Its affinity for the serotonin 5-HT2A receptor was about 15-fold lower than that ofDOB andDOI, whereas its affinity for the serotonin 5-HT1A receptor was the same as that of DOI and was about half that of DOB.[2] TFMBOX also very weaklyinhibited the reuptake of serotonin (IC50Tooltip half-maximal inhibitory concentration = 9,900 nM), but did not affectdopamine ornorepinephrinereuptake (IC50 = >50,000–100,000 nM).[2] The drug fully substituted forLSD in rodentdrug discrimination tests, albeit with about one-third of thepotency of DOB and2C-B.[2]

TFMBOX was first described in thescientific literature by Nick Cozzi, a student ofDavid E. Nichols, by 1994.[2][3] Other "BOX" drugs that were assessed by the group include BOX (the cyclized analogue of2C-H andDOH), BBOX (the cyclized analogue of 2C-B and DOB), and IBOX (the cyclized analogue of2C-I and DOI).[2][3] However, BBOX and IBOX only partially substituted for LSD in drug discrimination tests.[2][3][4]

See also

[edit]

References

[edit]
  1. ^abTrachsel 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. 852–853.ISBN 978-3-03788-700-4.OCLC 858805226. Retrieved31 January 2025.
  2. ^abcdefghiMonte AP, Marona-Lewicka D, Cozzi NV, Nelson DL, Nichols DE (1995)."Conformationally Restricted Tetrahydro-1-Benzoxepin Analogs of Hallucinogenic Phenethylamines".Medicinal Chemistry Research.5 (651–663).
  3. ^abcdCozzi NV (1994).Pharmacological studies of some psychoactive phenylalkylamines: Entactogens, hallucinogens, and anorectics (Ph.D. thesis). University of Wisconsin, Madison. Retrieved15 April 2025.
  4. ^Monte AP (August 1995).Structure-activity relationships of hallucinogens: Design, synthesis, and pharmacological evaluation of a series of conformationally restricted phenethylamines (Ph.D. thesis). Purdue University. Retrieved15 April 2025.

External links

[edit]
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
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
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
Retrieved from "https://en.wikipedia.org/w/index.php?title=TFMBOX&oldid=1322811371"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp