Benzenesulfonamides
![eMolecules 6209-17-2 | Sulfacetamide sodium salt hydrate | Combi-Blocks, Inc.254.240 | C8H11N2NaO4S | 98.000 | O.[Na+].CC(=O)[N-]S(=O)(=O)c1ccc(N)cc1 | 5g | 603146067](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502186680.JPG-250.jpg)
eMolecules 6209-17-2 | Sulfacetamide sodium salt hydrate | Combi-Blocks, Inc.254.240 | C8H11N2NaO4S | 98.000 | O.[Na+].CC(=O)[N-]S(=O)(=O)c1ccc(N)cc1 | 5g | 603146067
Sulfacetamide sodium salt hydrate | Combi-Blocks, Inc. | 6209-17-2254.240 | C8H11N2NaO4S | 98.000 | O.[Na+].CC(=O)[N-]S(=O)(=O)c1ccc(N)cc1 | 5g | 603146067
![eMolecules 171599-83-0 | SILDENAFIL CITRATE | AstaTech | MFCD09026931 | 666.700 | C28H38N6O11S | 95.000 | OC(=O)CC(O)(CC(O)=O)C(O)=O.CCCc1nn(C)c2c1nc([nH]c2=O)-c1cc(ccc1OCC)S(=O)(=O)N1CCN(C)CC1 | 25g | 410712234](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000162673.jpg-250.jpg)
eMolecules 171599-83-0 | SILDENAFIL CITRATE | AstaTech | MFCD09026931 | 666.700 | C28H38N6O11S | 95.000 | OC(=O)CC(O)(CC(O)=O)C(O)=O.CCCc1nn(C)c2c1nc([nH]c2=O)-c1cc(ccc1OCC)S(=O)(=O)N1CCN(C)CC1 | 25g | 410712234
SILDENAFIL CITRATE | AstaTech | 171599-83-0 | MFCD09026931 | 666.700 | C28H38N6O11S | 95.000 | OC(=O)CC(O)(CC(O)=O)C(O)=O.CCCc1nn(C)c2c1nc([nH]c2=O)-c1cc(ccc1OCC)S(=O)(=O)N1CCN(C)CC1 | 25g | 410712234
eMolecules 127191-97-3 | Medchem Express | KN-62 | 5mg | 446262681 | HY-13290 | MFCD00083180 | 721.85 | C38H35N5O6S2
Ambeed | 6-Chloro-5-(4-(1-hydroxycyclobutyl)phenyl)-1H-indole-3-carboxylic acid | 5mg | 552728241 | A421471 | 1467057-23-3 | MFCD29917835 | 341.790 | C19H16ClNO3
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eMolecules 108409-83-2 | Medchem Express | FH535 | 10mg | 446266435 | HY-15721 | MFCD01212888 | 361.19 | C13H10Cl2N2O4S
Ambeed | 6-Bromo-5-methyl-2H-benzo[b][14]oxazin-3(4H)-one | 250mg | 596568683 | A431223 | 1154740-47-2 | MFCD20527815 | 242.072 | C9H8BrNO2
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Medchemexpress LLC CD73-IN-3 | 2375815-63-5 | 99.89% | 286.33 | 50 MG
CD73-IN-3 is a potent CD73 inhibitor with an IC50 of 7.3 nM in a Calu6 human cell assay. This compound, derived from patent WO2019168744 A1, demonstrates potential utility in cancer research. In vitro studies show it effectively inhibits CD73 activity in human serum with an EC50 of 0.213 μM.
- Potent CD73 inhibitor with an IC50 of 7.3 nM in Calu6 human cell assays.
- Inhibits CD73 activity in human serum with an EC50 of 0.213 μM.
- Shows inhibition rates of 56.8%, 71.7%, and 76.9% at concentrations of 0.52 μM, 1.56 μM, and 4.68 μM.
- Potential for cancer research.
Medchemexpress LLC Sildenafil | 139755-83-2 | C22H30N6O4S | 50 MG
Sildenafil is a potent phosphodiesterase type 5 (PDE5) inhibitor with an IC50 of 5.22 nM. This compound is intended for research use only and is not sold to patients.
- Potent phosphodiesterase type 5 (PDE5) inhibitor
- Cited in numerous scientific publications
- Potentiates phosphorylation of ERK1/ERK2 and increases cell proliferation in vitro
- Significantly increases intracavernosal pressure in a dog model of erection
- Reduces microglia/macrophages in a pMCAo mouse model
- Decreases flap necrosis in preclinical animal models by increasing growth factors
- Under investigation in clinical trials for various conditions including Heart Failure and Erectile Dysfunction
eMolecules 680590-49-2 | EMPA | Axon Medchem | MFCD23381172 | 454.55 | C23H26N4O4S | 99 | CCN(Cc1cccnc1)C(=O)CN(c1ccc(OC)nc1)S(=O)(=O)c1ccccc1C | 10mg | 248227569
EMPA | Axon Medchem | 680590-49-2 | MFCD23381172 | 454.550 | C23H26N4O4S | 99.000 | CCN(Cc1cccnc1)C(=O)CN(c1ccc(OC)nc1)S(=O)(=O)c1ccccc1C | 10mg | 248227569
Enzo Life Sciences NBQX . disodium salt (25mg). CAS: 118876-58-7 (non-salt)
Water soluble, potent and selective AMPA/kainate receptor antagonist. For literature references, see NBQX (ALX-550-044). Alternative name: 2,3-Dihydroxy-6-nitro-7-sulphamoylbenzo(f)-quinoxaline . 2Na, 6-Nitro-7-sulphamoylbenzo(f)-quinoxaline-2,3-dione . 2Na. Purity: ≥98% (HPLC). Solubility: Soluble in water (5mg/ml) or DMSO. Long Term Storage: -20°C.
eMolecules 1899-94-1 | 3-Methylbenzenesulfonamide | Oakwood Chemicals | MFCD04066695 | 171.210 | C7H9NO2S | 98.000 | Cc1cccc(c1)S(N)(=O)=O | 25g | 480123629
3-Methylbenzenesulfonamide | Oakwood Chemicals | 1899-94-1 | MFCD04066695 | 171.210 | C7H9NO2S | 98.000 | Cc1cccc(c1)S(N)(=O)=O | 25g | 480123629
Frontier Specialty Chemicals 1G 1- (3-BROMOBENZENE)SULFONYL
1-[(3-Bromobenzene)sulfonyl]piperidine; CAS: 871269-12-4; 1g
Selleck Chemical LLC H-1152 dihydrochloride-5mg
H-1152 dihydrochloride (2HCl) is a membrane-permeable and selective inhibitor of Rho-associated protein kinase (ROCK). H-1152 inhibits ROCK2, PKA, PKC, PKG, AuroraA and CaMK2 with IC50 of 0.0120 μM, 3.03 μM, 5.68 μM, 0.360 μM, 0.745 μM and 0.180 μM, respectively.
Accela Chembio Inc 1-bromo-4-(phenylsulfonyl)benzene | 1g | 23038-36-0 | MFCD00034047 | 95+% | Shelf Life: 1260 Days | Light Sensitive
1-bromo-4-(phenylsulfonyl)benzene | 1g | 23038-36-0 | MFCD00034047 | 95+% | Shelf Life: 1260 Days | Light Sensitive
Medchemexpress LLC Abt-724 trihydrochloride | 587870-77-7 | 99.1% | 402.75 g/mol | C17H22Cl3N5 | 100 MG
ABT-724 trihydrochloride is a potent, selective dopamine D4 receptor agonist supplied for research use. It shows low-nanomolar activity at human D4 receptors and is used in pharmacological studies of dopaminergic signaling. The compound is provided as a solid, with defined purity and storage recommendations.
Accela Chembio Inc 3-bromobenzenesulfonamide | 25g | 89599-01-9 | MFCD00084903 | 97+% | Shelf Life: 900 Days | Light Sensitive/n2
3-bromobenzenesulfonamide | 25g | 89599-01-9 | MFCD00084903 | 97+% | Shelf Life: 900 Days | Light Sensitive/n2