Benzenesulfonamides
eMolecules 1258641-38-1 | Medchem Express | (Rac)-ABT-202 (dihydrochloride) | 5mg | 506403872 | HY-124540B | MFCD17480378 | 236.14 | C9H15Cl2N3
Ambeed | 2-Bromo-1-(2-chloro-6-methoxyphenyl)ethanone | 100mg | 600840608 | A447721 | 1427354-83-3 | MFCD23711724 | 263.520 | C9H8BrClO2
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eMolecules 376638-65-2 | Medchem Express | BVT-14225 | 5mg | 446268863 | HY-18055 | MFCD25976913 | 401.92 | C16H20ClN3O3S2
Ambeed | 4-Methoxy-2-oxo-12-dihydropyridine-3-carboxylic acid | 100mg | 626256599 | A147498 | 87853-70-1 | MFCD20654516 | 169.136 | C7H7NO4
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Medchemexpress LLC Glimepiride | 93479-97-1 | 99.9% | C24H34N4O5S | 500 MG
Glimepiride (Glimperide) is a medium-to-long acting sulfonylurea anti-diabetic compound. It acts mainly by stimulating insulin release from pancreatic beta cells and increasing the sensitivity to insulin at receptor sites, thereby lowering blood sugar. Glimepiride is effective in controlling blood glucose and is often used as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
- Medium-to-long acting anti-diabetic compound
- Stimulates insulin release from pancreatic beta cells
- Increases insulin sensitivity at receptor sites
- Effective in controlling blood glucose
- Used to improve glycemic control in type 2 diabetes mellitus
![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 | 100g | 410712235](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000159297.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 | 100g | 410712235
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 | 100g | 410712235
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 | 5g | 410712233
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 | 5g | 410712233
![eMolecules 2158-14-7 | 4-Acetamidobenzenesulfonyl Azide | Accela ChemBio (ASD) | MFCD00029626 | 240.240 | C8H8N4O3S | 97.000 | CC(=O)Nc1ccc(cc1)S(=O)(=O)N=[N+]=[N-] | 10g | 444748600](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000491665.jpg-250.jpg)
eMolecules 2158-14-7 | 4-Acetamidobenzenesulfonyl Azide | Accela ChemBio (ASD) | MFCD00029626 | 240.240 | C8H8N4O3S | 97.000 | CC(=O)Nc1ccc(cc1)S(=O)(=O)N=[N+]=[N-] | 10g | 444748600
4-Acetamidobenzenesulfonyl Azide | Accela ChemBio (ASD) | 2158-14-7 | MFCD00029626 | 240.240 | C8H8N4O3S | 97.000 | CC(=O)Nc1ccc(cc1)S(=O)(=O)N=[N+]=[N-] | 10g | 444748600
Medchemexpress LLC Rac-osmi-1 | 2748153-92-4 | 96.5% | 50 MG
Rac-OSMI-1 is the racemate of OSMI-1, a cell-permeable small-molecule inhibitor of O-GlcNAc transferase (OGT) used in cellular research to reduce protein O-linked N-acetylglucosamine (O-GlcNAc) modification.
- Inhibits O-GlcNAc transferase with reported IC50 ≈ 2.7 μM.
- Racemic small molecule for cellular research.
- Molecular weight 563.64 g/mol.
- Reported purity 96.5%.
- Available as a solid in a 50 mg package.
Medchemexpress LLC Sildenafil N-oxide | 1094598-75-0 | MFCD22683784 | 10mg
Sildenafil Impurity 1 is an impurity of Sildenafil (HY-15025)
Medchemexpress LLC Sulfacetamide sodium | 127-56-0 | 99.7% | 25 G
Sulfacetamide sodium is a sulfonamide antibiotic that can be used for the study of ocular infections. It exhibits antifungal and antibacterial activities.
- Used for the study of various ocular infections like trachoma, blepharitis, conjunctivitis, corneal ulcer, pityriasis versicolor, and rosacea
- Acts as an antifungal agent through a CYP51A1-independent mechanism
- Bacteriostatic agent with similar activity against both Gram-positive and Gram-negative bacteria
Medchemexpress LLC Sulfacetamide sodium monohydrate | 6209-17-2 | >99.5% | 10 G
Sulfacetamide sodium monohydrate is a sulfonamide antibiotic effective against ocular infections. It exhibits antifungal and antibacterial activities, making it suitable for studying conditions like trachoma, blepharitis, conjunctivitis, and corneal ulcers.
- Acts as an antifungal drug through a CYP51A1-independent mechanism
- Functions as a bacteriostatic agent
- Effective against both Gram-positive and Gram-negative bacteria
- Can be used for the study of various ocular infections
Medchemexpress LLC HY-12063 10mg Medchemexpress, PHT-427 CAS:1191951-57-1 Purity:>98%
Medchemexpress, HY-12063 10mg PHT-427 CAS:1191951-57-1 PHT-247 is an inhibitor of the pleckstrin homology (PH) domain of Akt, and it is also an inhibitor of PDPK1 with Kis of 2.7 µM and 5.2 µM and for Akt and PDPK1, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC Orexin receptor antagonist 3 | 1293282-55-9 | 99.6% | 434.45 | 50 MG
Orexin receptor antagonist 3 (example 216) is an orexin receptor antagonist, which is extracted from the patent WO2011050198A1. It is intended for research use only and not for sale to patients.
- Acts as an orexin receptor antagonist.
- Solid with an off-white to light yellow appearance.
- Solubility in DMSO is 33.33 mg/mL (76.72 mM).
- Storage recommendations include -20°C for 3 years as a powder, 4°C for 2 years as a powder, -80°C for 6 months in solvent, and -20°C for 1 month in solvent.
Selleck Chemical LLC Hydroxyhexamide
Hydroxyhexamide is a pharmacologically active metabolite of acetohexamide which is a sulfonylurea hypoglycemic agent
Medchemexpress LLC Probenecid | 57-66-9 | 99.94% | 500 MG
Probenecid is a potent and selective agonist for transient receptor potential vanilloid 2 (TRPV2) channels and acts as an inhibitor of pannexin 1 channels. It is widely utilized in research to study various biological processes.
- Potent and selective agonist of TRPV2 channels
- Inhibits pannexin 1 channels
- Efficiently inhibits ATP-dependent active vesicular NEM-GS uptake by MRP1 and MRP2
- Inhibitor of hTAS2R16, hTAS2R38, and hTAS2R43 bitter taste receptors
- Enhances cellular signals in GPCR calcium mobilization assays
- Increases contractility (ejection fraction, EF) in WT mice
- Involved in numerous clinical trials for various conditions