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Triflubazam

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
Triflubazam
Identifiers
  • 1-methyl-5-phenyl-7-(trifluoromethyl)-1H-1,5-benzodiazepine-2,4(3H,5H)-dione
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC17H13F3N2O2
Molar mass334.298 g·mol−1
3D model (JSmol)
  • FC(F)(C1=CC(N(C2=CC=CC=C2)C(CC(N3C)=O)=O)=C3C=C1)F
  • InChI=1S/C17H13F3N2O2/c1-21-13-8-7-11(17(18,19)20)9-14(13)22(16(24)10-15(21)23)12-5-3-2-4-6-12/h2-9H,10H2,1H3 checkY
  • Key:DMNPCIKBNDKNTO-UHFFFAOYSA-N checkY
  (verify)

Triflubazam[1] is a drug which is a 1,5-benzodiazepine derivative, related toclobazam.[2] It hassedative andanxiolytic effects, with a long half-life and duration of action.[3][4][5]

See also

[edit]

References

[edit]
  1. ^US 3660381, Karl-Heinz Weber KH, Merz H, K Zeile, Giesemann R, Danneberg P, "5-Aryl-1H-1,5-benzodiazepine-2,4-diones", issued 2 May 1972, assigned to CH Boehringer Sohn AG and Co KG 
  2. ^Lundbeck Institute (2003)."triflubazam". psychotropics.dk. Retrieved17 November 2010.
  3. ^Itil TM, Akpinar S, Fink M, Polvan N, Huque M, Sungurbey K (March 1976). "Controlled clinical and quantitative EEG studies of triflubazam (ORF 8063) in patients with anxiety syndrome".Current Therapeutic Research, Clinical and Experimental.19 (3):307–15.PMID 5248.
  4. ^Csanalosi I, Pereira-Oran J, Case G, et al. (1977). "Triflubazam (ORF 8063), a new benzodiazepine in anxiety neurosis".Current Therapeutic Research.22:166–171.
  5. ^Nicholson AN, Stone BM, Clarke CH (October 1977)."Effect of the 1,5-benzodiazepines, clobazam and triflubazam, on sleep in man".British Journal of Clinical Pharmacology.4 (5):567–72.doi:10.1111/j.1365-2125.1977.tb00787.x.PMC 1429140.PMID 20917.
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
Barbiturates
Benzodiazepines
Carbamates
Flavonoids
Imidazoles
Kava constituents
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Pyrazolopyridines
Quinazolinones
Volatiles/gases
Others/unsorted


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