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
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
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
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:32:20 GMT 2023
by
admin
on
Fri Dec 15 18:32:20 GMT 2023
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Record UNII |
80D8H0388T
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Record Status |
Validated (UNII)
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Record Version |
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-
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Code | English |
Classification Tree | Code System | Code | ||
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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
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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
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Code System | Code | Type | Description | ||
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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PRIMARY |
Related Record | Type | Details | ||
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ACTIVE MOIETY |