Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H13N3O3S |
| Molecular Weight | 267.304 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(C)C(NS(=O)(=O)C2=CC=C(N)C=C2)=NO1
InChI
InChIKey=DAUFGBIKKGOPJA-UHFFFAOYSA-N
InChI=1S/C11H13N3O3S/c1-7-8(2)17-13-11(7)14-18(15,16)10-5-3-9(12)4-6-10/h3-6H,12H2,1-2H3,(H,13,14)
| Molecular Formula | C11H13N3O3S |
| Molecular Weight | 267.304 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Sulfatroxazole is a sulfamide derivative patented by Swiss multinational healthcare company F. Hoffmann-La Roche & Co., A.-G. as an antibacterial agent and bacteriostatic antibiotic. Sulfatroxazole competitively inhibits dihydropteroate synthase preventing the formation of dihydropteroic acid, a precursor of folic acid which is required for bacterial growth. Sulfatroxazole is a component present in various veterinary drugs.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL4566 |
260.0 nM [IC50] | ||
Target ID: CHEMBL612490 Sources: https://www.ncbi.nlm.nih.gov/pubmed/3701916 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:40:25 GMT 2025
by
admin
on
Mon Mar 31 19:40:25 GMT 2025
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| Record UNII |
ZXC0PT8FFS
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| Record Status |
Validated (UNII)
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Official Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English |
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WHO-VATC |
QJ01EW14
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WHO-VATC |
QJ01EQ14
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NCI_THESAURUS |
C29739
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3362
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CHEMBL26630
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100000083784
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C048358
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DTXSID20177829
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C152459
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SUB10734MIG
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ZXC0PT8FFS
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31771
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23256-23-7
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245-530-5
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |