Benzenesulfonamides
Selleck Chemical LLC Zafirlukast ICI-204219-50mg
Zafirlukast (ICI-204219) is an oral leukotriene receptor antagonist (LTRA), used to prevent asthma symptoms.
eMolecules 20759-40-4 | 3-HYDROXYBENZENESULFONAMIDE | MFCD16999679 | 1g
AstaTech | 4-METHYL-2-PYRIDIN-3-YL-THIAZOLE-5-CARBOXYLIC ACID | 5g | 112528156 | 64017 | 97.000 | 39091-01-5 | MFCD00171753 | 220.250 | C10H8N2O2S
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Medchemexpress LLC Rac-osmi-1 | 2748153-92-4 | 96.5% | 5 MG
(Rac)-OSMI-1 is the racemic form of OSMI-1, a cell-permeable small-molecule inhibitor of O-GlcNAc transferase (OGT) used in biochemical and cell-based research to reduce protein O-GlcNAcylation.
- Cell-permeable OGT inhibitor with reported IC50 ≈ 2.7 μM.
- Suitable for cell-based assays and biochemical studies.
- Purity approximately 96.5% (manufacturer-stated).
- Molecular weight 563.64 g/mol; formula C28H25N3O6S2.
- Research-use only; not for clinical or human use.
Medchemexpress LLC Pci-27483 | 871266-63-6 | 99.10% | 596.57 | 100 MG
Pci-27483 | 871266-63-6 | 99.10% | 596.57 | 100 MG
Medchemexpress LLC Furosemide sodium | 41733-55-5 | MFCD23379919 | 99.9% | 500 MG
Furosemide sodium is a potent and orally active inhibitor of Na+/K+/2Cl- (NKCC) cotransporter, specifically NKCC1 and NKCC2. It also acts as a GABAA receptors antagonist, exhibiting 100-fold selectivity for α6-containing receptors over α1-containing receptors. This compound functions as a loop diuretic and is utilized in the study of congestive heart failure, hypertension, and edema. It is intended for research use only and is not sold to patients.
- Potent and orally active inhibitor of NKCC1 and NKCC2 cotransporters
- Functions as a GABAA receptors antagonist
- Exhibits 100-fold selectivity for α6-containing receptors over α1-containing receptors
- Acts as a loop diuretic
- Used in studies of congestive heart failure, hypertension, and edema
- Intended for research use only
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.
eMolecules 658084-23-2 | Medchem Express | SU11274 | 5mg | 673358807 | HY-12014 | 568.09 | C28H30ClN5O4S
Medchem Express | SU11274 | 5mg | 673358807 | HY-12014 | 658084-23-2 | 568.090 | C28H30ClN5O4S
eMolecules 150725-87-4 | Medchem Express | Ro 46-2005 | 5mg | 446269889 | HY-19529 | MFCD00918670 | 473.54 | C23H27N3O6S
Ambeed | (35-Difluoro-4-propoxyphenyl)boronic acid | 100mg | 717401517 | A363125 | 2096331-43-8 | MFCD20231441 | 215.990 | C9H11BF2O3
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Medchemexpress LLC Oregon green 488 azide | 2648246-11-9 | 98.0% | 637.67 | C33H37F2N5O6 | 10 MG
Oregon Green 488 azide is a green-fluorescent azide reagent used to label alkyne-modified biomolecules via copper-catalyzed azide-alkyne cycloaddition (click chemistry). It is supplied as a solid dye with high purity for biochemical assays and fluorescence labeling.
- Bright green-fluorescent azide probe for click chemistry.
- Reacts selectively with terminal alkynes via copper-catalyzed azide-alkyne cycloaddition.
- High purity (98.0%) suitable for biochemical assays.
- Solid, orange to red appearance for easy handling and storage.
- Storage: sealed, away from moisture and light; in solvent: -80°C (6 months), -20°C (1 month).
- Available in multiple pack sizes, including 10 MG.
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.
Medchemexpress LLC Glimepiride | 93479-97-1 | 99.9% | C24H34N4O5S | 10 MM * 1 ML
Glimepiride is a medium-to-long acting sulfonylurea anti-diabetic compound with an ED50 of 182 μg/kg. It is for research use only. It has been shown to decrease extracellular Aβ40 and Aβ42 levels, potentially serving as a promising drug for the treatment of AD associated with diabetes. Compared to other sulfonylureas, it is generally associated with a lower risk of hypoglycemia and less weight gain, and may be safer for patients with cardiovascular disease due to its lack of detrimental effects on ischemic preconditioning.
- Medium-to-long acting sulfonylurea anti-diabetic compound
- Lowers blood glucose in rabbits more effectively than glibenclamide
- Associated with lower risk of hypoglycemia and less weight gain
- May be safer for patients with cardiovascular disease
Sigma Aldrich Fine Chemicals Biosciences Chlorthalidone >=98% (HPLC) | 77-36-1 | 5MG
Chlorthalidone >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 338.77 | 77-36-1 | 5MG
eMolecules 1457940-75-8 | Medchem Express | Orexin receptor antagonist 2 | 5mg | 572596842 | HY-136922 | 433.556 | C25H31N5O2
Medchem Express | Dihydrolapachenole | 1mg | 536985023 | HY-N7638 | 20213-26-7 | MFCD03084173 | 242.318 | C16H18O2
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