CAS 121-61-9
:N-Acetylsulfanilamide
Description:
N-Acetylsulfanilamide, with the CAS number 121-61-9, is a sulfonamide compound that exhibits both antibacterial and anti-inflammatory properties. It is a white to off-white crystalline powder that is soluble in water and organic solvents, making it useful in various pharmaceutical applications. The compound features an acetyl group attached to the amino group of sulfanilamide, which enhances its pharmacological activity. N-Acetylsulfanilamide is primarily known for its role as a precursor in the synthesis of other sulfonamide drugs and has been studied for its potential therapeutic effects. Its mechanism of action typically involves the inhibition of bacterial folic acid synthesis, which is crucial for bacterial growth and replication. Additionally, this compound may exhibit mild analgesic properties. However, like many sulfonamides, it can cause allergic reactions in some individuals, and its use should be monitored for potential side effects. Overall, N-Acetylsulfanilamide is significant in medicinal chemistry and continues to be of interest in drug development.
Formula:C8H10N2O3S
InChI:InChI=1/C8H10N2O3S/c1-6(11)10-7-2-4-8(5-3-7)14(9,12)13/h2-5H,1H3,(H,10,11)(H2,9,12,13)
InChI key:InChIKey=PKOFBDHYTMYVGJ-UHFFFAOYSA-N
SMILES:S(N)(=O)(=O)C1=CC=C(NC(C)=O)C=C1
Synonyms:- 4-Acetamidobenzenesulfonamide
- 4-Acetylaminobenzenesulfonamide
- 4-Acetylaminobenzensulfonamide
- 4-Sulfamoylacetanilide
- A-319
- Acetamide, N-[4-(aminosulfonyl)phenyl]-
- Acetanilide, 4′-sulfamoyl-
- Acetylsulfanilamide
- Benzenesulfonamide, 4-(acetylamino)-
- Erytrin
- N-(4-sulfamoylphenyl)acetamide
- N-4-Acetylsulfanilamide
- N-[4-(Aminosulfonyl)phenyl]acetamide
- N4-acetylsulfanilamide
- N<sup>4</sup>-Acetsulfanilamide
- N<sup>4</sup>-Acetylsulfanilamide
- NSC 217
- NSC 406839
- Neotherapol
- N′-Acetylsulphanilamide
- Sulfanilamide-N<sup>4</sup>-acetate
- p-(Acetylamino)benzenesulfonamide
- p-Acetamidobenzenesulfonamide
- p-Sulfamoylacetanilide
- p-Sulfamylacetanilide
- N-(4-SULFAMOYL-PHENYL)-ACETAMIDE
- n-(4-(aminosulfonyl)phenyl)-acetamid
- ACETSULPHANILAMIDE
- 4’-sulfamoyl-acetanilid
- n(sup4)-acetylsulfanilamide
- N-ACETYLSULFANILAMIDE
- n-(4-sulfamylphenyl)acetamide
- P-ACETYLAMINOBENZENESULFONAMIDE
- N4-ACETYL SULPHANILAMIDE
- See more synonyms
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Found 10 products.
4-Acetamidobenzenesulfonamide
CAS:Formula:C8H10N2O3SPurity:>98.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalMolecular weight:214.244-Acetamidobenzenesulfonamide
CAS:Formula:C8H10N2O3SPurity:98%Color and Shape:SolidMolecular weight:214.2416p-Sulfamylacetanilide
CAS:Formula:C8H10N2O3SColor and Shape:White To Off-White SolidMolecular weight:214.244-Acetamidobenzenesulfonamide
CAS:4-AcetamidobenzenesulfonamidePurity:≥98%Molecular weight:214.24g/mol4-Acetamidobenzenesulfonamide
CAS:<p>4-Acetamidobenzenesulfonamide used in proteomics research and is an anti-infective agent</p>Formula:C8H10N2O3SPurity:99.86%Color and Shape:Solid Solid CrystallineMolecular weight:214.244'-Sulphamoylacetanilide
CAS:4'-SulphamoylacetanilideFormula:C8H10N2O3SPurity:≥95%Color and Shape: white solidMolecular weight:214.24g/molp-Sulfamylacetanilide
CAS:Controlled Product<p>Applications p-Sulfamylacetanilide has been used as an inhibitor of mitochondrial isoenzyme carbonic anhydrase V inhibitiors. Vullo, Daniela<br>References Vullo, D. et al.: J. Med. Chem., 47, 1272 (2004);<br></p>Formula:C8H10N2O3SColor and Shape:NeatMolecular weight:214.24N-(4-Sulfamoylphenyl)acetamide
CAS:Formula:C8H10N2O3SPurity:98%Color and Shape:SolidMolecular weight:214.244-Acetamidobenzenesulfonamide
CAS:<p>4-Acetamidobenzenesulfonamide is a drug that inhibits the activity of several enzymes and is used in wastewater treatment. It has been shown to have a beneficial effect on metabolic disorders, such as insulin resistance, obesity, and type 2 diabetes. 4-Acetamidobenzenesulfonamide also regulates transcriptional activity by inhibiting the interaction between DNA and RNA polymerases. This drug has been shown to be active in treating autoimmune diseases, such as multiple sclerosis, rheumatoid arthritis, lupus erythematosus and Crohn's disease. It also aids in HIV infection by acting as an inhibitor of toll-like receptor signalling pathways. The drug binds to hydrogen bonds and hydrophobic interactions with water molecules to form a hydrophobic layer on the surface of cells in order to reduce water permeability. The drug also reduces bowel diseases such as ulcerative colitis and liver lesions caused by alcohol consumption or congestive</p>Formula:C8H10N2O3SPurity:Min. 95%Molecular weight:214.24 g/mol








