U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C12H14O2S2
Molecular Weight 254.368
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DITOPHAL

SMILES

CCSC(=O)C1=CC(=CC=C1)C(=O)SCC

InChI

InChIKey=DWGXUDUOJPYAOR-UHFFFAOYSA-N
InChI=1S/C12H14O2S2/c1-3-15-11(13)9-6-5-7-10(8-9)12(14)16-4-2/h5-8H,3-4H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C12H14O2S2
Molecular Weight 254.368
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Ditophal was used for the treatment of leprosy.

Approval Year

PubMed

PubMed

TitleDatePubMed
Chemotherapeutic trials in leprosy. 2. Comparative trial of dapsone plus ditophal (Etisul) and dapsone alone in the treatment of lepromatous leprosy.
1965-07-01
DISTRIBUTION, METABOLISM AND EXCRETION OF PERCUTANEOUSLY ADMINISTERED DITOPHAL ("ETISUL").
1965-02
Ditophal in the treatment of leprosy.
1962-01
Action of two ethyl thiol esters against experimental tuberculosis in the guinea-pig.
1960-03

Sample Use Guides

Unknown
Route of Administration: Topical
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:17:50 GMT 2025
Edited
by admin
on Mon Mar 31 18:17:50 GMT 2025
Record UNII
40SR2754GL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
S,S-DIETHYL 1,3-DITHIOISOPHTHALATE
Preferred Name English
DITOPHAL
INN  
INN  
Official Name English
ditophal [INN]
Common Name English
S,S-DIETHYL ESTER OF 1,3-DITHIOISOPHTHALIC ACID
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C258
Created by admin on Mon Mar 31 18:17:50 GMT 2025 , Edited by admin on Mon Mar 31 18:17:50 GMT 2025
Code System Code Type Description
PUBCHEM
3083635
Created by admin on Mon Mar 31 18:17:50 GMT 2025 , Edited by admin on Mon Mar 31 18:17:50 GMT 2025
PRIMARY
WIKIPEDIA
DITOPHAL
Created by admin on Mon Mar 31 18:17:50 GMT 2025 , Edited by admin on Mon Mar 31 18:17:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID40207112
Created by admin on Mon Mar 31 18:17:50 GMT 2025 , Edited by admin on Mon Mar 31 18:17:50 GMT 2025
PRIMARY
INN
894
Created by admin on Mon Mar 31 18:17:50 GMT 2025 , Edited by admin on Mon Mar 31 18:17:50 GMT 2025
PRIMARY
EVMPD
SUB06336MIG
Created by admin on Mon Mar 31 18:17:50 GMT 2025 , Edited by admin on Mon Mar 31 18:17:50 GMT 2025
PRIMARY
CAS
584-69-0
Created by admin on Mon Mar 31 18:17:50 GMT 2025 , Edited by admin on Mon Mar 31 18:17:50 GMT 2025
PRIMARY
NCI_THESAURUS
C65445
Created by admin on Mon Mar 31 18:17:50 GMT 2025 , Edited by admin on Mon Mar 31 18:17:50 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104300
Created by admin on Mon Mar 31 18:17:50 GMT 2025 , Edited by admin on Mon Mar 31 18:17:50 GMT 2025
PRIMARY
SMS_ID
100000081860
Created by admin on Mon Mar 31 18:17:50 GMT 2025 , Edited by admin on Mon Mar 31 18:17:50 GMT 2025
PRIMARY
FDA UNII
40SR2754GL
Created by admin on Mon Mar 31 18:17:50 GMT 2025 , Edited by admin on Mon Mar 31 18:17:50 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY