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

Details

Stereochemistry ACHIRAL
Molecular Formula C17H15Cl2N3O5S
Molecular Weight 444.289
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULAZURIL

SMILES

CN1CC(=O)NC(=O)N1C2=CC(Cl)=C(OC3=CC=C(C=C3)S(C)(=O)=O)C(Cl)=C2

InChI

InChIKey=AQAZEGOUFUGKBP-UHFFFAOYSA-N
InChI=1S/C17H15Cl2N3O5S/c1-21-9-15(23)20-17(24)22(21)10-7-13(18)16(14(19)8-10)27-11-3-5-12(6-4-11)28(2,25)26/h3-8H,9H2,1-2H3,(H,20,23,24)

HIDE SMILES / InChI

Molecular Formula C17H15Cl2N3O5S
Molecular Weight 444.289
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulazuril (also known as Hoe 092 V) is a phenyltriazolone derivative patented by Hoechst A.-G. as agrochemical protozoacide. Sulazuril is effective against a broad spectrum of fish and crustacean parasites.

Approval Year

PubMed

PubMed

TitleDatePubMed
Hoe 092 V, a new triazine derivative effective against a broad spectrum of fish and crustacean parasites.
1992
Patents

Sample Use Guides

fish: 2.5 micrograms V/ml
Route of Administration: Topical
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:27:43 GMT 2023
Edited
by admin
on Sat Dec 16 17:27:43 GMT 2023
Record UNII
2136B7T7KE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULAZURIL
INN  
INN  
Official Name English
sulazuril [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C250
Created by admin on Sat Dec 16 17:27:43 GMT 2023 , Edited by admin on Sat Dec 16 17:27:43 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID30148469
Created by admin on Sat Dec 16 17:27:43 GMT 2023 , Edited by admin on Sat Dec 16 17:27:43 GMT 2023
PRIMARY
NCI_THESAURUS
C72602
Created by admin on Sat Dec 16 17:27:43 GMT 2023 , Edited by admin on Sat Dec 16 17:27:43 GMT 2023
PRIMARY
SMS_ID
100000083236
Created by admin on Sat Dec 16 17:27:43 GMT 2023 , Edited by admin on Sat Dec 16 17:27:43 GMT 2023
PRIMARY
EVMPD
SUB10675MIG
Created by admin on Sat Dec 16 17:27:43 GMT 2023 , Edited by admin on Sat Dec 16 17:27:43 GMT 2023
PRIMARY
CAS
108258-89-5
Created by admin on Sat Dec 16 17:27:43 GMT 2023 , Edited by admin on Sat Dec 16 17:27:43 GMT 2023
PRIMARY
INN
6604
Created by admin on Sat Dec 16 17:27:43 GMT 2023 , Edited by admin on Sat Dec 16 17:27:43 GMT 2023
PRIMARY
FDA UNII
2136B7T7KE
Created by admin on Sat Dec 16 17:27:43 GMT 2023 , Edited by admin on Sat Dec 16 17:27:43 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105474
Created by admin on Sat Dec 16 17:27:43 GMT 2023 , Edited by admin on Sat Dec 16 17:27:43 GMT 2023
PRIMARY
PUBCHEM
65904
Created by admin on Sat Dec 16 17:27:43 GMT 2023 , Edited by admin on Sat Dec 16 17:27:43 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY