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Details

Stereochemistry ACHIRAL
Molecular Formula C32H34N4O4S
Molecular Weight 570.702
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of DIATHYMOSULFONE

SMILES

CC(C)C1=C(O)C=C(C)C(=C1)\N=N\C2=CC=C(C=C2)S(=O)(=O)C3=CC=C(C=C3)\N=N\C4=CC(C(C)C)=C(O)C=C4C

InChI

InChIKey=KHFUQWURHSKTPO-LBYUQGKWSA-N
InChI=1S/C32H34N4O4S/c1-19(2)27-17-29(21(5)15-31(27)37)35-33-23-7-11-25(12-8-23)41(39,40)26-13-9-24(10-14-26)34-36-30-18-28(20(3)4)32(38)16-22(30)6/h7-20,37-38H,1-6H3/b35-33+,36-34+

HIDE SMILES / InChI

Molecular Formula C32H34N4O4S
Molecular Weight 570.702
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 2
Optical Activity NONE

Diathymosulfone is an antibacterial agent. It was used as antimycobacterial and leprostatic drug.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Contributions to the treatment of tuberculosis with combined Timosulfone and INH].
1965
[OUR EXPERIENCES WITH DIATHYMOSULFONE + ISONIAZID TREATMENT IN VARIOUS FORMS OF TUBERCULOSIS].
1963-06
[Severe relapse of a lepromatous leper treated for six years by the sulfone J-51].
1959-08-29
[Treatment of tuberculosis in the diabetic with sulfone J. 51 (thymosulfone)].
1958-04
[Thymosulfone in the treatment of leprosy].
1957-01
[Remote results of treatment of leprosy by the sulfone J-51; presentation of patients].
1956-07-01
[Trial combined treatment of leprosy by the sulfone J-51 at the Leproserie Saint-Antoine de Harar].
1956-07-01
[Results of the clinical study of the use of the sulfone J-51 (thymosulfone) in the treatment of pulmonary and osteoarticular tuberculosis].
1955-12
[Treatment of pulmonary tuberculosis with the sulfone J. 51].
1955-02
[Sulfone J. 51 in the treatment of leprosy; mode of action].
1955
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:19:33 GMT 2025
Edited
by admin
on Mon Mar 31 18:19:33 GMT 2025
Record UNII
UK27RQ38IX
Record Status Validated (UNII)
Record Version
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Name Type Language
DIATHYMOSULFONE
INN   MI  
INN  
Official Name English
DIATHYMOSULFONE [MI]
Preferred Name English
DI(4-(4-HYDROXY-2-METHYL-5-ISOPROPYLPHENYLAZO)PHENYL)SULFONE
Systematic Name English
DI(4-(4-HYDROXY-2-METHYL-5-ISOPROPYLPHENYLAZO)PHENYL)SULPHONE
Systematic Name English
DIATHYMOSULPHONE
Common Name English
diathymosulfone [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C849
Created by admin on Mon Mar 31 18:19:33 GMT 2025 , Edited by admin on Mon Mar 31 18:19:33 GMT 2025
Code System Code Type Description
CAS
5964-62-5
Created by admin on Mon Mar 31 18:19:33 GMT 2025 , Edited by admin on Mon Mar 31 18:19:33 GMT 2025
PRIMARY
ChEMBL
CHEMBL2106611
Created by admin on Mon Mar 31 18:19:33 GMT 2025 , Edited by admin on Mon Mar 31 18:19:33 GMT 2025
PRIMARY
EVMPD
SUB07067MIG
Created by admin on Mon Mar 31 18:19:33 GMT 2025 , Edited by admin on Mon Mar 31 18:19:33 GMT 2025
PRIMARY
SMS_ID
100000082905
Created by admin on Mon Mar 31 18:19:33 GMT 2025 , Edited by admin on Mon Mar 31 18:19:33 GMT 2025
PRIMARY
DRUG CENTRAL
3726
Created by admin on Mon Mar 31 18:19:33 GMT 2025 , Edited by admin on Mon Mar 31 18:19:33 GMT 2025
PRIMARY
NCI_THESAURUS
C77131
Created by admin on Mon Mar 31 18:19:33 GMT 2025 , Edited by admin on Mon Mar 31 18:19:33 GMT 2025
PRIMARY
INN
738
Created by admin on Mon Mar 31 18:19:33 GMT 2025 , Edited by admin on Mon Mar 31 18:19:33 GMT 2025
PRIMARY
FDA UNII
UK27RQ38IX
Created by admin on Mon Mar 31 18:19:33 GMT 2025 , Edited by admin on Mon Mar 31 18:19:33 GMT 2025
PRIMARY
EPA CompTox
DTXSID201024233
Created by admin on Mon Mar 31 18:19:33 GMT 2025 , Edited by admin on Mon Mar 31 18:19:33 GMT 2025
PRIMARY
MERCK INDEX
m682
Created by admin on Mon Mar 31 18:19:33 GMT 2025 , Edited by admin on Mon Mar 31 18:19:33 GMT 2025
PRIMARY Merck Index
Related Record Type Details
ACTIVE MOIETY