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Fletazepam

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Fletazepam
Clinical data
ATC code
  • none
Identifiers
  • 7-chloro-5-(2-fluorophenyl)-1-(2,2,2-trifluoroethyl)-2,3-dihydro-1,4-benzodiazepine
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
ECHA InfoCard100.047.309Edit this at Wikidata
Chemical and physical data
FormulaC17H13ClF4N2
Molar mass356.75 g·mol−1
3D model (JSmol)
  • FC1=CC=CC=C1C2=NCCN(CC(F)(F)F)C3=C2C=C(Cl)C=C3
  • InChI=1S/C17H13ClF4N2/c18-11-5-6-15-13(9-11)16(12-3-1-2-4-14(12)19)23-7-8-24(15)10-17(20,21)22/h1-6,9H,7-8,10H2 checkY
  • Key:CIZCSUNUBQXVFP-UHFFFAOYSA-N checkY
  (verify)

Fletazepam[1] is a drug which is abenzodiazepine derivative. It hassedative andanxiolytic effects similar to those produced by other benzodiazepine derivatives, but is mainly notable for its strongmuscle relaxant properties.[2]

Fletazepam is most closely related to otherN-trifluoroethyl substituted benzodiazepines such ashalazepam andquazepam.[3]

See also

[edit]

References

[edit]
  1. ^DE 2106175, Steinmann, Martin, "Neue 1-Polyfluoralkylbenzodiazepine und Verfahren zu ihrer Herstellung [Novel 1-polyfluoroalkylbenzodiazepines and processes for their preparation]", published 1971-09-30, assigned toSherico Ltd. 
  2. ^Barnett A, Goldstein J, Fiedler EP, Taber RI (November 1974). "The pharmacology of fletazepam a centrally-acting muscle relaxant".Archives Internationales de Pharmacodynamie et de Therapie.212 (1):164–74.PMID 4476200.
  3. ^Iorio LC, Barnett A, Billard W (July 1984). "Selective affinity of 1-N-trifluoroethyl benzodiazepines for cerebellar type 1 receptor sites".Life Sciences.35 (1):105–13.doi:10.1016/0024-3205(84)90157-7.PMID 6738302.
1,4-Benzodiazepines
1,5-Benzodiazepines
2,3-Benzodiazepines*
Triazolobenzodiazepines
Imidazobenzodiazepines
Oxazolobenzodiazepines
Thienodiazepines
Thienotriazolodiazepines
Thienobenzodiazepines*
Pyridodiazepines
Pyridotriazolodiazepines
Pyrazolodiazepines
Pyrrolodiazepines
Tetrahydroisoquinobenzodiazepines
Pyrrolobenzodiazepines*
Benzodiazepine prodrugs
* atypical activity profile (notGABAA receptor ligands)
Alcohols
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Benzodiazepines
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Flavonoids
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Kava constituents
Monoureides
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Nonbenzodiazepines
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