Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H9N3O2S2 |
| Molecular Weight | 231.295 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=S)NS(=O)(=O)C1=CC=C(N)C=C1
InChI
InChIKey=UEMLYRZWLVXWRU-UHFFFAOYSA-N
InChI=1S/C7H9N3O2S2/c8-5-1-3-6(4-2-5)14(11,12)10-7(9)13/h1-4H,8H2,(H3,9,10,13)
| Molecular Formula | C7H9N3O2S2 |
| Molecular Weight | 231.295 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/21024878Curator's Comment: description was created based on several sources, including
http://www.ncbi.nlm.nih.gov/pubmed/13137202
Sources: http://www.ncbi.nlm.nih.gov/pubmed/21024878
Curator's Comment: description was created based on several sources, including
http://www.ncbi.nlm.nih.gov/pubmed/13137202
Sulphathiourea (Badional) is short acting sulfonamide, belongs to antibacterial drugs
Approval Year
Sample Use Guides
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/24544024
Tests of capacity to inhibit growth showed sulphathiourea to be inferior to sulphadimetine for most Gram-negative organisms except Shigella, but superior to it in its action on Gram-positive organisms, notably haemolytic streptococci and staphylococci. Sulphathiourea is bactericidal when added to a culture in the early stages of growth
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:10:54 GMT 2025
by
admin
on
Mon Mar 31 18:10:54 GMT 2025
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| Record UNII |
MXF9G4I1V5
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| Record Status |
Validated (UNII)
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WHO-ATC |
J01EB08
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NCI_THESAURUS |
C29739
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108228
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C025270
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3567
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3000579
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DTXSID4046868
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CHEMBL2107489
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m10345
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SUB10732MIG
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100000083783
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DB13699
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Sulfathiourea
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C76982
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515-49-1
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MXF9G4I1V5
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208-201-7
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4161
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |