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Details

Stereochemistry RACEMIC
Molecular Formula C17H17NO2
Molecular Weight 267.3224
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETAZEPINE

SMILES

CCOC1C2=CC=CC=C2N(C)C(=O)C3=C1C=CC=C3

InChI

InChIKey=BLGFGFHRMMDRPC-UHFFFAOYSA-N
InChI=1S/C17H17NO2/c1-3-20-16-12-8-4-5-9-13(12)17(19)18(2)15-11-7-6-10-14(15)16/h4-11,16H,3H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C17H17NO2
Molecular Weight 267.3224
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Etazepine (5,6-dihydro-5-methyl-11H-11-ethoxy-dibenzo[b,e]azepin-6-one) demonstrates anticonvulsant activity in rodents. Etazepine seems to exert its anticonvulsant effects by activating the GABAergic system.

CNS Activity

Curator's Comment: Etazepine is CNS active in animals. No human data available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacological profile of the new anticonvulsant etazepine.
1989 Apr
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:45:46 UTC 2023
Edited
by admin
on Sat Dec 16 17:45:46 UTC 2023
Record UNII
SBC76K7XWC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETAZEPINE
INN  
INN  
Official Name English
etazepine [INN]
Common Name English
(±)-11-ETHOXY-5,11-DIHYDRO-5-METHYL-6H-DIBENZ(B,E)AZEPIN-6-ONE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C264
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
Code System Code Type Description
INN
5533
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
EPA CompTox
DTXSID10868996
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
EVMPD
SUB07266MIG
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
WIKIPEDIA
Etazepine
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
CAS
88124-27-0
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
MESH
C060314
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
FDA UNII
SBC76K7XWC
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
SMS_ID
100000082391
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
NCI_THESAURUS
C65556
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
PUBCHEM
65662
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
ChEMBL
CHEMBL2106559
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
ECHA (EC/EINECS)
289-386-1
Created by admin on Sat Dec 16 17:45:47 UTC 2023 , Edited by admin on Sat Dec 16 17:45:47 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY