| 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 |
MOL RATIO
1 MOL RATIO (average) |
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
Patents
Sample Use Guides
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
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SALT/SOLVATE -> PARENT | |||
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SALT/SOLVATE -> PARENT |
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