Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H9N3O2S2 |
| Molecular Weight | 255.317 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC=C(S1)S(=O)(=O)C2=CC=C(N)C=C2
InChI
InChIKey=KVEZIRCKNOTGKY-UHFFFAOYSA-N
InChI=1S/C9H9N3O2S2/c10-6-1-3-7(4-2-6)16(13,14)8-5-12-9(11)15-8/h1-5H,10H2,(H2,11,12)
| Molecular Formula | C9H9N3O2S2 |
| Molecular Weight | 255.317 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Thiazosulfone (also known as Promizole) is a phenylsulfonylthiazole derivative patented by Parke, Davis & Co. as the anti-tuberculosis agent. In preclinical models, Thiazosulfone exerts a definitely favorable influence on the course of experimental tuberculosis previously established in the highly susceptible guinea pig. In clinical trials Thiazosulfone and Streptomycin combined therapy exerts favor influences on tuberculous meningitis. Thiazosulfone seems to have an inhibitory action on hematogenous tuberculosis. Its toxicity is very low and it can, therefore, be administered for a prolonged period.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15405408
from 1 to 1.5 G
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:43:13 GMT 2025
by
admin
on
Wed Apr 02 09:43:13 GMT 2025
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| Record UNII |
WE45JZI7YO
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| Record Status |
Validated (UNII)
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| Record Version |
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C849
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m10731
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C152587
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SUB10972MIG
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100000082418
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CHEMBL2107139
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473-30-3
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C009453
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DTXSID80197088
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |