U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C17H10Cl2N4O2
Molecular Weight 373.193
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLAZURIL

SMILES

ClC1=CC=C(C=C1)C(C#N)C2=CC=C(C=C2Cl)N3N=CC(=O)NC3=O

InChI

InChIKey=QUUTUGLQZLNABV-UHFFFAOYSA-N
InChI=1S/C17H10Cl2N4O2/c18-11-3-1-10(2-4-11)14(8-20)13-6-5-12(7-15(13)19)23-17(25)22-16(24)9-21-23/h1-7,9,14H,(H,22,24,25)

HIDE SMILES / InChI

Molecular Formula C17H10Cl2N4O2
Molecular Weight 373.193
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Clazuril is benzene-acetonitrile derivative, developed by Janssen Pharmaceutica as an anticoccidial agent for the treatment of pigeons. The anticoccidial effect is due to a cidal effect on the endogenous stages of the Eimeria species.

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:59:30 GMT 2023
Edited
by admin
on Fri Dec 15 15:59:30 GMT 2023
Record UNII
O8W0R05772
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLAZURIL
INN   MART.   MI   USAN  
USAN   INN  
Official Name English
R62,690
Code English
CLAZURIL [MART.]
Common Name English
clazuril [INN]
Common Name English
BENZENEACETONITRILE, 2-CHLORO-.ALPHA.-(4-CHLOROPHENYL)-4-(4,5-DIHYDRO-3,5-DIOXO-1,2,4-TRIAZIN-2(3H)-YL)-
Systematic Name English
R-62690
Code English
CLAZURIL [USAN]
Common Name English
CLAZURIL, (±)-
Common Name English
(±)-CLAZURIL
Common Name English
CLAZURIL [MI]
Common Name English
(2-CHLORO-4-(4,5-DIHYDRO-3,5-DIOXO-AS-TRIAZIN-2(3H)-YL)PHENYL)(P-CHLOROPHENYL)ACETONITRILE
Common Name English
Classification Tree Code System Code
WHO-VATC QP51AJ02
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
Code System Code Type Description
MERCK INDEX
m3611
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY Merck Index
FDA UNII
O8W0R05772
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
WIKIPEDIA
CLAZURIL
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
MESH
C056172
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
NCI_THESAURUS
C82246
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
CAS
101831-36-1
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
USAN
Y-60
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID30869364
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104190
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
SMS_ID
100000080171
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
PUBCHEM
58901
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
EVMPD
SUB06645MIG
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
INN
5970
Created by admin on Fri Dec 15 15:59:30 GMT 2023 , Edited by admin on Fri Dec 15 15:59:30 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY