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Details

Stereochemistry RACEMIC
Molecular Formula C12H10ClN3O
Molecular Weight 247.68
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ZONICLEZOLE

SMILES

CC(N1C=CN=C1)C2=NOC3=C2C=C(Cl)C=C3

InChI

InChIKey=QMKRARTVXMQOBW-UHFFFAOYSA-N
InChI=1S/C12H10ClN3O/c1-8(16-5-4-14-7-16)12-10-6-9(13)2-3-11(10)17-15-12/h2-8H,1H3

HIDE SMILES / InChI

Molecular Formula C12H10ClN3O
Molecular Weight 247.68
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Zoniclezole was proven to have anticonvulsant profile. It is representative of a novel class of water-soluble agents being developed for the treatment of epilepsy. Zoniclezole has been shown to be a potential antagonist of electroshock-induced seizures in animals, and to some degree, pentylenetetrazol-induced seizures. In preclinical studies the compound had prolonged efficacy at relatively low doses. Zoniclezole is glutamate receptor antagonist.

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:21:01 GMT 2025
Edited
by admin
on Mon Mar 31 18:21:01 GMT 2025
Record UNII
H1C5F0K79E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ZONICLEZOLE
INN  
INN  
Official Name English
zoniclezole [INN]
Preferred Name English
5-CHLORO-3-(1-IMIDAZOL-1-YLETHYL)-1,2-BENZISOXAZOLE
Systematic Name English
1,2-BENZISOXAZOLE, 5-CHLORO-3-(1-(1H-IMIDAZOL-1-YL)ETHYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C264
Created by admin on Mon Mar 31 18:21:01 GMT 2025 , Edited by admin on Mon Mar 31 18:21:01 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID20869671
Created by admin on Mon Mar 31 18:21:01 GMT 2025 , Edited by admin on Mon Mar 31 18:21:01 GMT 2025
PRIMARY
MESH
C078649
Created by admin on Mon Mar 31 18:21:01 GMT 2025 , Edited by admin on Mon Mar 31 18:21:01 GMT 2025
PRIMARY
SMS_ID
100000078799
Created by admin on Mon Mar 31 18:21:01 GMT 2025 , Edited by admin on Mon Mar 31 18:21:01 GMT 2025
PRIMARY
FDA UNII
H1C5F0K79E
Created by admin on Mon Mar 31 18:21:01 GMT 2025 , Edited by admin on Mon Mar 31 18:21:01 GMT 2025
PRIMARY
PUBCHEM
60745
Created by admin on Mon Mar 31 18:21:01 GMT 2025 , Edited by admin on Mon Mar 31 18:21:01 GMT 2025
PRIMARY
ChEMBL
CHEMBL2111150
Created by admin on Mon Mar 31 18:21:01 GMT 2025 , Edited by admin on Mon Mar 31 18:21:01 GMT 2025
PRIMARY
CAS
121929-20-2
Created by admin on Mon Mar 31 18:21:01 GMT 2025 , Edited by admin on Mon Mar 31 18:21:01 GMT 2025
PRIMARY
EVMPD
SUB00186MIG
Created by admin on Mon Mar 31 18:21:01 GMT 2025 , Edited by admin on Mon Mar 31 18:21:01 GMT 2025
PRIMARY
INN
6912
Created by admin on Mon Mar 31 18:21:01 GMT 2025 , Edited by admin on Mon Mar 31 18:21:01 GMT 2025
PRIMARY
NCI_THESAURUS
C82235
Created by admin on Mon Mar 31 18:21:01 GMT 2025 , Edited by admin on Mon Mar 31 18:21:01 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY