Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C16H18N2O4S |
| Molecular Weight | 334.39 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)OC1=CC=C(C=C1)C(=O)NS(=O)(=O)C2=CC=C(N)C=C2
InChI
InChIKey=FBFBRAFXKGRRHI-UHFFFAOYSA-N
InChI=1S/C16H18N2O4S/c1-11(2)22-14-7-3-12(4-8-14)16(19)18-23(20,21)15-9-5-13(17)6-10-15/h3-11H,17H2,1-2H3,(H,18,19)
Sulfaproxyline is a sulfonamide derivative patented by J. R. Geigy A.-G. as an antibiotic, useful in the treatment of urinary tract infections. In preclinical models, sulfaproxyline is effective against staphylococci infection in guinea pigs. Bisulfon D, a drug product comprising the combination of sulfaproxyline and sulfamerazine has been used for the treatment of urinary tract infections in the puerperium.
Approval Year
| Name | Type | Language | ||
|---|---|---|---|---|
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Official Name | English | ||
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Common Name | English | ||
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Code | English | ||
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Common Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C255
Created by
admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
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NCI_THESAURUS |
C29739
Created by
admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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100000083276
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116-42-7
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204-140-5
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301
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DTXSID70861746
Created by
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PRIMARY | |||
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C72855
Created by
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PRIMARY | |||
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SUB10722MIG
Created by
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PRIMARY | |||
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CHEMBL2107520
Created by
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PRIMARY | |||
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C052571
Created by
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PRIMARY | |||
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120646
Created by
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YR841R53VW
Created by
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PRIMARY | |||
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m10337
Created by
admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
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PRIMARY | Merck Index | ||
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67002
Created by
admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
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PRIMARY |
ACTIVE MOIETY
