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Details

Stereochemistry ACHIRAL
Molecular Formula C7H10N2O2S.C7H9N3O2S2
Molecular Weight 417.527
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFATOLAMIDE

SMILES

NCC1=CC=C(C=C1)S(N)(=O)=O.NC(=S)NS(=O)(=O)C2=CC=C(N)C=C2

InChI

InChIKey=ZLYHTQKHXIVMLY-UHFFFAOYSA-N
InChI=1S/C7H9N3O2S2.C7H10N2O2S/c8-5-1-3-6(4-2-5)14(11,12)10-7(9)13;8-5-6-1-3-7(4-2-6)12(9,10)11/h1-4H,8H2,(H3,9,10,13);1-4H,5,8H2,(H2,9,10,11)

HIDE SMILES / InChI

Molecular Formula C7H9N3O2S2
Molecular Weight 231.295
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C7H10N2O2S
Molecular Weight 186.231
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulfatolamide is a combination of two sulfonamide antibacterials, sulfathiourea and mafenide, previously used in the treatment of gynecological infections.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Results of capillary fragilometry, and changes in blood coagulation after intraperitoneal instillation and marbadal].
1954
Patents

Sample Use Guides

vaginal tablets
Route of Administration: Vaginal
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:20:10 UTC 2023
Edited
by admin
on Sat Dec 16 16:20:10 UTC 2023
Record UNII
3OLH2HAK9F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFATOLAMIDE
INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
SULFATOLAMIDE [MI]
Common Name English
sulfatolamide [INN]
Common Name English
SULFATOLAMIDE [MART.]
Common Name English
Sulfatolamide [WHO-DD]
Common Name English
SULFATOLAMIDE [JAN]
Common Name English
Classification Tree Code System Code
WHO-ATC G01AE01
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
WHO-VATC QG01AE01
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
NCI_THESAURUS C2166
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
Code System Code Type Description
ECHA (EC/EINECS)
214-600-7
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
EVMPD
SUB10733MIG
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
WIKIPEDIA
SULFATOLAMIDE
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
DRUG CENTRAL
4724
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
CAS
1161-88-2
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
EPA CompTox
DTXSID90151277
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
MERCK INDEX
m486
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY Merck Index
INN
861
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
NCI_THESAURUS
C76983
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
MESH
C009350
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
PUBCHEM
3034019
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
DRUG BANK
DB13547
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
SMS_ID
100000083764
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
FDA UNII
3OLH2HAK9F
Created by admin on Sat Dec 16 16:20:11 UTC 2023 , Edited by admin on Sat Dec 16 16:20:11 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE