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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T14953 | Chloroquinoxaline sulfonamide | NSC-339004,Chloroquinoxaline | Topoisomerase |
Chloroquinoxaline sulfonamide is a topoisomerase II alpha/beta poison. It is used to control coccidiosis in poultry, rabbit, sheep, and cattle. | |||
T0571 | 2-Methylbenzene-1-sulfonamide | Others | |
2-Methylbenzene-1-sulfonamide is used for saccharin, pharmaceutical intermediates, etc. | |||
T77607 | WAY-604663 | 2,3-diphenylquinoxaline-6-sulfonamide | Antibiotic |
WAY-604663 (2,3-diphenylquinoxaline-6-sulfonamide) may have antibacterial analgesic and anti-inflammatory activities. | |||
T8590 | 4-(benzyloxy)benzene-1-sulfonamide | Others | |
4-(benzyloxy)benzene-1-sulfonamide is inhibitor of human recombinant CA-7. | |||
T8611 | 2,3-dihydro-1H-indene-5-sulfonamide | Carbonic Anhydrase | |
2,3-dihydro-1H-indene-5-sulfonamide is Carbonic anhydrase 12 (human) inhibitor. | |||
T6781 | Benzenesulfonamide | Benzenesulphonamide,Phenyl sulfonamide,Benzosulfonamide | Carbonic Anhydrase |
Benzenesulfonamide (Benzosulfonamide) ia an inhibitor of carbonic anhydrases. | |||
T50062 | 2,5-dichloro-4-(difluoromethoxy)-N,N-dimethylbenzene-1-sulfonamide | PDE | |
2,5-dichloro-4-(difluoromethoxy)-N,N-dimethylbenzene-1-sulfonamide is a PDE inhibitor. | |||
T3214 | NS-398 | N-(2-cyclohexyloxy-4-nitrophenyl)methane sulfonamide,NS398 | COX |
NS-398 (N-(2-cyclohexyloxy-4-nitrophenyl)methane sulfonamide) is a COX-2 inhibitor wih anti-inflammatory activity. | |||
T50056 | 4-(4,5-dibromo-6-oxo-1,6-dihydropyridazin-1-yl)benzene-1-sulfonamide | Others | |
4-(4,5-dibromo-6-oxo-1,6-dihydropyridazin-1-yl)benzene-1-sulfonamide is a sulfonamide derivative used in the synthesis of building blocks for various supramolecular structures such as metal-organic skeletons and coordina... | |||
T23525 | W-9 hydrochloride | N-(6-aminohexyl)-5-chloronaphthalene-2-sulfonamide hydrochloride | CaMK |
W-9 hydrochloride is a calmodulin antagonist. | |||
T60054 | EJMC-1 | N-(3-chloro-4-hydroxyphenyl)-2-oxo-1,2-dihydrobenzo[cd]indole-6-sulfonamide | TNF |
EJMC-1 is an inhibitor of TNF-α with an IC50 value of 42 μM and can be used in studies about auto-inflammatory diseases. | |||
T64332 | Glimepiride sulfonamide | Immunology/Inflammation related | |
Glimepiride sulfonamide is an antiinflammatory agent. | |||
T23469 | TQS | 4-Naphthalen-1-yl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline-8-sulfonamide | AChR |
TQS (4-Naphthalen-1-yl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline-8-sulfonamide) is a positive allosteric modulator of α7 nACh receptors. | |||
T77724 | OBHSA | Oxabicycloheptane sulfonamide | Estrogen/progestogen Receptor |
OBHSA(Oxabicycloheptane sulfonamide) is a novel selective estrogen receptor depressant (SERD) that can be used to study breast cancer. | |||
T15438 | GSK3186899 | 3,3,3-trifluoro-N-[4-[[3-[(2R)-2-methylmorpholin-4-yl]-1H-pyrazolo[3,4-d]pyrimidin-6-yl]amino]cyclohexyl]propane-1-sulfonamide,DDD-853651 | Parasite |
GSK3186899 is an inhibitor of Cdc2-related kinase 12 with an EC50 of 1.4 μM for L. donovani. | |||
T10441 | Azosemide | Na-K-Cl cotransporter | |
Azosemide is a potent NKCC1 inhibitor (IC50s: 0.246 µM and 0.197 µM for hNKCC1A and NKCC1B). | |||
T0930 | Sulfadiazine | Sulphadiazine | Antibacterial , Antibiotic , Parasite , Autophagy |
Sulfadiazine (Sulphadiazine) is a synthetic pyrimidinyl sulfonamide derivative, short-acting bacteriostatic Sulfadiazine inhibits bacterial folic acid synthesis by competing with para-aminobenzoic acid. It is used in com... | |||
T0747 | Sulfathiazole | 2-Sulfanilamidothiazole | Antibacterial , Antibiotic , Autophagy |
Sulfathiazole (2-Sulfanilamidothiazole), an organosulfur compound, has been served as a short-acting sulfa medicine. | |||
T0510 | Sulfaguanidine | Sulfaguine,Guanicil | Antibacterial , Antibiotic , Autophagy |
Sulfaguanidine (Guanicil), a sulfonamide, is served as an anti-infective agent. | |||
T0699 | Sulfamonomethoxine | Antibacterial , Antibiotic | |
Sulfamonomethoxine is a long-acting sulfonamide antibacterial agent, blocks the synthesis of folic acid by inhibiting synthetase of dihydropteroate. |