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Details

Stereochemistry ACHIRAL
Molecular Formula C10H9ClN4O2S
Molecular Weight 284.722
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFACLOZINE

SMILES

NC1=CC=C(C=C1)S(=O)(=O)NC2=CN=CC(Cl)=N2

InChI

InChIKey=QKLPUVXBJHRFQZ-UHFFFAOYSA-N
InChI=1S/C10H9ClN4O2S/c11-9-5-13-6-10(14-9)15-18(16,17)8-3-1-7(12)2-4-8/h1-6H,12H2,(H,14,15)

HIDE SMILES / InChI

Molecular Formula C10H9ClN4O2S
Molecular Weight 284.722
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including: http://en.kimiafaam.com/allp/p/coc/10.php | http://www.bela-pharm.com/nc/produkte/gefluegel.html?download=Sulfaclozin-Na_60_prozent-K068-1209.pdf

SULFACLOZINE is a competitive antagonist of para-aminobenzoic acid (PABA), a precursor of folic acid, in protozoa and bacteria. It is indicated for treatment of coccidiosis in poultry due to infection with Eimeria species, fowl typhoid due to infection with Salmonella gallinarum and fowl cholera due to infection with Pasteurella multocida. Adverse reactions are liver damage, allergic reactions. In poultry undesirable effects, as inappetence, diarrhoea, growth depression, or haemorrhages after administration of sulfaclozine are rare. Prolong use may cause crystal urea.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
ESB3

Approved Use

ESB 3 is indicated for treatment of coccidiosis in poultry due to infection with Eimeria species, fowl typhoid due to infection with Salmonella gallinarum and fowl cholera due to infection with Pasteurella multocida. It can be also used for coccidiosis treatment in Lambs, Calves and Rabbit.
Curative
ESB3

Approved Use

ESB 3 is indicated for treatment of coccidiosis in poultry due to infection with Eimeria species, fowl typhoid due to infection with Salmonella gallinarum and fowl cholera due to infection with Pasteurella multocida. It can be also used for coccidiosis treatment in Lambs, Calves and Rabbit.
Curative
ESB3

Approved Use

ESB 3 is indicated for treatment of coccidiosis in poultry due to infection with Eimeria species, fowl typhoid due to infection with Salmonella gallinarum and fowl cholera due to infection with Pasteurella multocida. It can be also used for coccidiosis treatment in Lambs, Calves and Rabbit.
PubMed

PubMed

TitleDatePubMed
[Action of sodium sulfachlorpyrazine (ESB3) on the endogenous development of Eimeria tenella in the experimental infestation of chickens].
1983
Effect of sulfachloropyrazine in the drinking water of chickens infected experimentally with fowl cholera.
1974-07
[Combination of anticoccidial drugs: experimental studies of the efficacy of the sulfachloropyrazine-diaveridine-ethopabate combination in the prevention of avian coccidiosis].
1974-04-01
[Effectiveness of sulfachlorpyrazine in coccidiosis of rabbits].
1973-04
Patents

Sample Use Guides

Poultry: Dissolve 1g Sulfaclozine (Sulfachloropyrazine) sodium monohydrate 30% per liter water. This provides approximately 50 mg active ingredient, or 170 mg Sulfaclozine (Sulfachloropyrazine) sodium monohydrate, per kg bodyweight. Treat for 3 consecutive days and repeat after a 2 days break if necessary (Shuttle programs like day 1, 3, 5, 7, 9 or 1, 2, 5, 6, 9 have also been found effective). · For coccidiosis in chicken caused by E. tenella and E. necatrix doses of 1.5g to 2.0g are indicated (75-100 g in 50 liters of drinking water). · For the treatment of cholera and typhoid, doses of 1 to 2 g Sulfaclozine (Sulfachloropyrazine) sodium monohydrate per liter water for at least 5 days are required. Sheep and Goats: 120 mg Sulfaclozine per kg body weight (Dissolve a full sachet in 1 liter drinking water and administer 12 ml for each 10kg Body weight).
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Wed Apr 02 07:44:52 GMT 2025
Edited
by admin
on Wed Apr 02 07:44:52 GMT 2025
Record UNII
69YP7Z48CW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFACLOZINE
INN   MART.  
INN  
Official Name English
ESB3
Preferred Name English
SULFACHLOROPYRAZINE
Common Name English
sulfaclozine [INN]
Common Name English
SULFATYF
Common Name English
N(SUP 1)-(6-CHLOROPYRAZINYL)SULFANILAMIDE
Systematic Name English
N(SUP 1)-(1-(M-CHLOROPHENYL)-3-METHYL-5-PYRAZOLYL)SULFANILAMIDE
Systematic Name English
ESB-3
Code English
SULFACLOZINE [MART.]
Common Name English
Classification Tree Code System Code
WHO-VATC QP51AG04
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
CFR 21 CFR 520.2184
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID60144515
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
MESH
C014199
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
CHEBI
145370
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
CAS
102-65-8
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
FDA UNII
69YP7Z48CW
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
INN
3030
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105493
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-044-0
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
SMS_ID
100000083244
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
EVMPD
SUB10693MIG
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
NCI_THESAURUS
C72849
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
PUBCHEM
66890
Created by admin on Wed Apr 02 07:44:52 GMT 2025 , Edited by admin on Wed Apr 02 07:44:52 GMT 2025
PRIMARY
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