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
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)
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
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL3242 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27144971 |
0.52 nM [Ki] | ||
Target ID: CHEMBL3510 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27144971 |
6.1 nM [Ki] | ||
Target ID: CHEMBL3594 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27144971 |
12.8 nM [Ki] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Sulfasuccinamide Approved UseApplied topically in the treatment of local infections of the ear, nose, and throat. |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27144971
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).
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NCI_THESAURUS |
C29739
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ACTIVE MOIETY