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Details

Stereochemistry RACEMIC
Molecular Formula C18H13ClFN3O2
Molecular Weight 357.766
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CINOLAZEPAM

SMILES

OC1N=C(C2=CC=CC=C2F)C3=CC(Cl)=CC=C3N(CCC#N)C1=O

InChI

InChIKey=XAXMYHMKTCNRRZ-UHFFFAOYSA-N
InChI=1S/C18H13ClFN3O2/c19-11-6-7-15-13(10-11)16(12-4-1-2-5-14(12)20)22-17(24)18(25)23(15)9-3-8-21/h1-2,4-7,10,17,24H,3,9H2

HIDE SMILES / InChI

Molecular Formula C18H13ClFN3O2
Molecular Weight 357.766
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Cinolazepam is a drug which is a benzodiazepine derivative. It possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. Cinolazepam is not approved for sale in the United States or Canada. Cinolazepam binds to central benzodiazepine receptors, which interact allosterically with GABA receptors. This potentiates the effects of the inhibitory neurotransmitter GABA, increasing the inhibition of the ascending reticular activating system and blocking the cortical and limbic arousal that occurs following stimulation of the reticular pathways. Statistical analyses of objective sleep variables in men demonstrated a significant improvement of sleep maintenance after cinolazepam as reflected by an increase of sleep efficiency, decrease of wake time (during total sleep period) and number of awakenings as compared with the placebo. It is indicated for the treatment of sleep disorders of different etiologies.

Approval Year

Sample Use Guides

The usual adult dose is 1 tablet (40 mg). The product is not suitable for long-term treatment. There is currently no experimental data on treatments longer than 3 weeks.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:48:31 GMT 2023
Edited
by admin
on Sat Dec 16 17:48:31 GMT 2023
Record UNII
68P0556B0U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CINOLAZEPAM
INN   MART.   MI   WHO-DD  
INN  
Official Name English
cinolazepam [INN]
Common Name English
CINOLAZEPAM [MART.]
Common Name English
CINOLAZEPAM [MI]
Common Name English
GERODORM
Brand Name English
Cinolazepam [WHO-DD]
Common Name English
7-CHLORO-5-(O-FLUOROPHENYL)-2,3-DIHYDRO-3-HYDROXY-2-OXO-1H-1,4-BENZODIAZEPINE-1-PROPIONITRILE
Common Name English
(±)-CINOLAZEPAM
Common Name English
CINOLAZEPAM, (±)-
Common Name English
Classification Tree Code System Code
WHO-ATC N05CD13
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
NCI_THESAURUS C1012
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
WHO-VATC QN05CD13
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
Code System Code Type Description
MERCK INDEX
m1073
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY Merck Index
PUBCHEM
3033621
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
WIKIPEDIA
CINOLAZEPAM
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
CHEBI
59514
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
FDA UNII
68P0556B0U
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104926
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
INN
5051
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
MESH
C053781
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
SMS_ID
100000081050
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
EVMPD
SUB06307MIG
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
DRUG BANK
DB01594
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
DRUG CENTRAL
656
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
NCI_THESAURUS
C77635
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
CAS
75696-02-5
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
EPA CompTox
DTXSID30868372
Created by admin on Sat Dec 16 17:48:31 GMT 2023 , Edited by admin on Sat Dec 16 17:48:31 GMT 2023
PRIMARY
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ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
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ACTIVE MOIETY