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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
Structure of SUBATHIZONE

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+

HIDE SMILES / InChI

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.

Approval Year

PubMed

PubMed

TitleDatePubMed
A study on the prolonged administration of p-ethylsulfonylbenzaldehyde-thiosemicarbazone for tuberculosis.
1953 Jun
Patents

Patents

Sample Use Guides

1 to 2 mg. twice daily.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:22:28 GMT 2023
Edited
by admin
on Fri Dec 15 16:22:28 GMT 2023
Record UNII
BSC36V44TK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SUBATHIZONE
INN   MI  
INN  
Official Name English
subathizone [INN]
Common Name English
NSC-718
Code English
SUBATHIZONE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C280
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
Code System Code Type Description
CAS
121-55-1
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
MESH
C004888
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
FDA UNII
BSC36V44TK
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
MERCK INDEX
m484
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY Merck Index
DRUG CENTRAL
3832
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-480-4
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
PUBCHEM
6474578
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
NCI_THESAURUS
C72606
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
EVMPD
SUB10661MIG
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107521
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
SMS_ID
100000083486
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
INN
98
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
EPA CompTox
DTXSID20861756
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
NSC
718
Created by admin on Fri Dec 15 16:22:28 GMT 2023 , Edited by admin on Fri Dec 15 16:22:28 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY