Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H13N3O2S2 |
| Molecular Weight | 271.359 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCS(=O)(=O)C1=CC=C(C=C1)\C=N\NC(N)=S
InChI
InChIKey=VUSKMERTTCJJPM-KPKJPENVSA-N
InChI=1S/C10H13N3O2S2/c1-2-17(14,15)9-5-3-8(4-6-9)7-12-13-10(11)16/h3-7H,2H2,1H3,(H3,11,13,16)/b12-7+
| Molecular Formula | C10H13N3O2S2 |
| Molecular Weight | 271.359 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Subathizone (also known as Berculon B) is a thiosemicarbazone derivative useful for the chemotherapy of tuberculosis. In preclinical models, Subathizone shows potent activity in experimental tuberculosis in the mouse. In clinical trial, Subathizone shows moderate efficacy and frequent adverse events. Gastrointestinal disturbances and progressive anemia were the most toxic effects, but liver dysfunction, malaise, depression and lassitude, exanthemata, and conjunctival irritation also occurred.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13080595
1 to 2 mg. twice daily.
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:26:22 GMT 2025
by
admin
on
Mon Mar 31 18:26:22 GMT 2025
|
| Record UNII |
BSC36V44TK
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C280
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
121-55-1
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
C004888
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
BSC36V44TK
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
m484
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | Merck Index | ||
|
3832
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
204-480-4
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
6474578
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
C72606
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
SUB10661MIG
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
CHEMBL2107521
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
100000083486
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
98
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
DTXSID20861756
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY | |||
|
718
Created by
admin on Mon Mar 31 18:26:22 GMT 2025 , Edited by admin on Mon Mar 31 18:26:22 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |