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Details

Stereochemistry ACHIRAL
Molecular Formula C10H12N2O5S
Molecular Weight 272.278
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFASUCCINAMIDE

SMILES

NS(=O)(=O)C1=CC=C(NC(=O)CCC(O)=O)C=C1

InChI

InChIKey=RXXXPZYBZLDQKP-UHFFFAOYSA-N
InChI=1S/C10H12N2O5S/c11-18(16,17)8-3-1-7(2-4-8)12-9(13)5-6-10(14)15/h1-4H,5-6H2,(H,12,13)(H,14,15)(H2,11,16,17)

HIDE SMILES / InChI
Sulfasuccinamide is a sulfonamide antibacterial with properties similar to those of sulfamethoxazole. It has been applied topically in the treatment of local infections of the ear, nose, and throat. It has also been given as the sodium salt. Sulfasuccinamide is a carbonic anhydrase inhibitor.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.52 nM [Ki]
6.1 nM [Ki]
12.8 nM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Sulfasuccinamide

Approved Use

Applied topically in the treatment of local infections of the ear, nose, and throat.
PubMed

PubMed

TitleDatePubMed
PEGylated Bis-Sulfonamide Carbonic Anhydrase Inhibitors Can Efficiently Control the Growth of Several Carbonic Anhydrase IX-Expressing Carcinomas.
2016 May 26

Sample Use Guides

Nasal solution
Route of Administration: Nasal
Sulfasuccinamide inhibited human recombinant carbonic anhydrase 12 with Ki value of 0.52 nM. Sulfasuccinamide decreased tumor cell viability of colon HT-29 cells in a concentration-dependent manner (0.01 - 1 mM).
Name Type Language
SULFASUCCINAMIDE
INN   MART.   WHO-DD  
INN  
Official Name English
NSC-30143
Code English
sulfasuccinamide [INN]
Common Name English
Sulfasuccinamide [WHO-DD]
Common Name English
SULFASUCCINAMIDE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29739
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
Code System Code Type Description
CAS
3563-14-2
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107036
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
PRIMARY
INN
4582
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
PRIMARY
EVMPD
SUB10729MIG
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
PRIMARY
FDA UNII
8286I9062N
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
PRIMARY
NCI_THESAURUS
C76981
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
PRIMARY
ECHA (EC/EINECS)
222-632-8
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
PRIMARY
SMS_ID
100000083762
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
PRIMARY
PUBCHEM
60582
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
PRIMARY
EPA CompTox
DTXSID5046275
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
PRIMARY
NSC
30143
Created by admin on Fri Dec 15 15:50:34 GMT 2023 , Edited by admin on Fri Dec 15 15:50:34 GMT 2023
PRIMARY