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
SMILES
NC1=CC=C(C=C1)S(=O)(=O)NC2=NC=C(Cl)N=C2
InChI
InChIKey=GDANWVKBBCWCIJ-UHFFFAOYSA-N
InChI=1S/C10H9ClN4O2S/c11-9-5-14-10(6-13-9)15-18(16,17)8-3-1-7(12)2-4-8/h1-6H,12H2,(H,14,15)
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 |
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/5331040
Curator's Comment: reference was retrieved from https://www.jstage.jst.go.jp/article/jpsa1964/11/3/11_3_75/_pdf
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
[Effectiveness of sulfachlorpyrazine in coccidiosis of rabbits]. | 1973 Apr |
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[The compatibility of the new ionophore-coccidiostats with other chemotherapeutics in broilers]. | 1989 Oct |
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Comparative studies on the efficacy of sulphachlorpyrazine and toltrazuril for the treatment of caecal coccidiosis in chickens. | 1995 Jun |
Patents
Sample Use Guides
chicken and turkey: 0.03% sulfachlorpyrazine solution as source of water for 3 days.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23682263
T. gondii tachyzoites were soaked in sulfachloropyrazine (250 mg/mL) for 2 h at 37 °C.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:44:32 GMT 2023
by
admin
on
Fri Dec 15 19:44:32 GMT 2023
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Record UNII |
96R84UZ2XA
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Record Status |
Validated (UNII)
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Record Version |
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