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Details

Stereochemistry ACHIRAL
Molecular Formula C17H13F3N2O2
Molecular Weight 334.2925
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIFLUBAZAM

SMILES

CN1C2=C(C=C(C=C2)C(F)(F)F)N(C3=CC=CC=C3)C(=O)CC1=O

InChI

InChIKey=DMNPCIKBNDKNTO-UHFFFAOYSA-N
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

HIDE SMILES / InChI

Molecular Formula C17H13F3N2O2
Molecular Weight 334.2925
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Triflubazam is a 1,5-benzodiazepine derivative. The hypnotic activity of the 1,5-benzodiazepines is limited, and that this is particularly so in the case of triflubazam. Subjects reported impaired sleep with triflubazam (40 mg), and a sense of less wakefulness the morning. The effect of triflubazam may have persisted beyond the night of ingestion. No effect of triflubazam was observed on total sleep time, stage shifts in the first 6 h or latency to the first rapid eye movement period of sleep. Triflubazam has psychopharmacological properties in animals suggestive of antianxiety activity of a longer duration than that of diazepam. The metabolism of triflubazam by man is characterized by extensive N-demethylation, aromatic hydroxylation, aromatic O-methylation and dihydrodiol formation.

Approval Year

PubMed

PubMed

TitleDatePubMed
A novel one-pot three-(in situ five-)component condensation reaction: an unexpected approach for the synthesis of tetrahydro-2,4-dioxo-1H-benzo[b][1,5]diazepine-3-yl-2-methylpropanamide derivatives.
2009 Aug 6
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:32:20 GMT 2023
Edited
by admin
on Fri Dec 15 18:32:20 GMT 2023
Record UNII
80D8H0388T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIFLUBAZAM
INN   USAN  
INN   USAN  
Official Name English
1H-1,5-BENZODIAZEPINE-2,4(3H,5H)-DIONE, 1-METHYL-5-PHENYL-7-(TRIFLUOROMETHYL)-
Systematic Name English
WE-352
Code English
TRIFLUBAZAM [USAN]
Common Name English
ORF-8063
Code English
triflubazam [INN]
Common Name English
WE352
Code English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
NCI_THESAURUS C28197
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C152743
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
PRIMARY
WIKIPEDIA
TRIFLUBAZAM
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
PRIMARY
SMS_ID
100000077723
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
PRIMARY
INN
3261
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107285
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
PRIMARY
EVMPD
SUB11285MIG
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
PRIMARY
CAS
22365-40-8
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
PRIMARY
FDA UNII
80D8H0388T
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID40176899
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
PRIMARY
PUBCHEM
31157
Created by admin on Fri Dec 15 18:32:20 GMT 2023 , Edited by admin on Fri Dec 15 18:32:20 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY