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Details

Stereochemistry RACEMIC
Molecular Formula C17H20N4O.ClH
Molecular Weight 332.828
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROPIZEPINE HYDROCHLORIDE

SMILES

Cl.CC(CN1C2=CC=CC=C2NC3=NC=CC=C3C1=O)N(C)C

InChI

InChIKey=DNZVNKSQOUOBOY-UHFFFAOYSA-N
InChI=1S/C17H20N4O.ClH/c1-12(20(2)3)11-21-15-9-5-4-8-14(15)19-16-13(17(21)22)7-6-10-18-16;/h4-10,12H,11H2,1-3H3,(H,18,19);1H

HIDE SMILES / InChI
Propizepine is a benzodiazepinone derivative patented by Laboratoires U.P.S.A. as antidepressive, antihistaminic, antianaphylactic, thymoanaleptic, antiserotonine, antispasmodic, and analgetic compound. Propizepine used in France for the treatment of depression in the 1970s.

Approval Year

PubMed

PubMed

TitleDatePubMed
Method development for a pyridobenzodiazepine library with multiple diversification points.
2008-02-12
Recent advances in the solid-phase combinatorial synthetic strategies for the benzodiazepine based privileged structures.
2006-01
Effects of JL13, a pyridobenzoxazepine with potential atypical antipsychotic activity, in animal models for schizophrenia.
2001-07
Effects of long-term treatment of rats with antidepressants on adrenergic-receptor sensitivity in cerebral cortex: Structure activity study.
1983
Patents
Name Type Language
PROPIZEPINE HYDROCHLORIDE
MI  
Common Name English
VAGRAN
Preferred Name English
UP-106
Code English
PROPIZEPINE HYDROCHLORIDE [MI]
Common Name English
5H-PYRIDO(2,3-B)(1,5)BENZODIAZEPIN-5-ONE, 6-(2-(DIMETHYLAMINO)PROPYL)-6,11-DIHYDRO-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
FDA UNII
Z5MO8L6XHR
Created by admin on Mon Mar 31 22:24:32 GMT 2025 , Edited by admin on Mon Mar 31 22:24:32 GMT 2025
PRIMARY
MERCK INDEX
m9216
Created by admin on Mon Mar 31 22:24:32 GMT 2025 , Edited by admin on Mon Mar 31 22:24:32 GMT 2025
PRIMARY Merck Index
CAS
14559-79-6
Created by admin on Mon Mar 31 22:24:32 GMT 2025 , Edited by admin on Mon Mar 31 22:24:32 GMT 2025
PRIMARY
PUBCHEM
3082068
Created by admin on Mon Mar 31 22:24:32 GMT 2025 , Edited by admin on Mon Mar 31 22:24:32 GMT 2025
PRIMARY
EPA CompTox
DTXSID30932648
Created by admin on Mon Mar 31 22:24:32 GMT 2025 , Edited by admin on Mon Mar 31 22:24:32 GMT 2025
PRIMARY
ECHA (EC/EINECS)
238-603-8
Created by admin on Mon Mar 31 22:24:32 GMT 2025 , Edited by admin on Mon Mar 31 22:24:32 GMT 2025
PRIMARY