Organosulfur Compounds
eMolecules N-(4,6-Dimethylpyrimidin-2-yl)-N-methylbenzene-1,4-diamine | 220844-79-1 | MFCD00202978 | 1g
Oakwood Chemical | N-(4,6-Dimethylpyrimidin-2-yl)-N-methylbenzene-1,4-diamine | 1g | 537681275 | 023699 | | 220844-79-1 | MFCD00202978 | 228.299 | C13H16N4
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eMolecules Ambeed / 26-Dimethylpyrimidin-4-amine / 10g / 490551093 / A296440 / / 461-98-3 / MFCD00006106 / 123.159 / C6H9N3
Ambeed / 26-Dimethylpyrimidin-4-amine / 10g / 490551093 / A296440 / / 461-98-3 / MFCD00006106 / 123.159 / C6H9N3
eMolecules 4-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid | 5934-14-5 | MFCD00864826 | 1g
Ambeed | 4-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid | 1g | 503282134 | A244444 | | 5934-14-5 | MFCD00864826 | 348.370 | C16H16N2O5S
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Medchemexpress LLC Mouse IgG2a Fc Isot 5mg | 5mg
Mouse IgG2a Fc Isotype Control is a Fc fragment of mouse IgG2a only and does not contain the Fab fragments The molecular mass is about 52 kDa
eMolecules 4,6-Dimethylpyrimidin-5-amine | 90856-77-2 | MFCD09834647 | 1g
Ambeed | 4,6-Dimethylpyrimidin-5-amine | 1g | 525175137 | A293869 | | 90856-77-2 | MFCD09834647 | 123.159 | C6H9N3
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Medchemexpress LLC Mouse IgG2a Fc Isot 1mg | 1mg
Mouse IgG2a Fc Isotype Control is a Fc fragment of mouse IgG2a only and does not contain the Fab fragments The molecular mass is about 52 kDa
Research Products International Corp Ertapenem Sodium Salt, 5 Grams
Ertapenem Sodium Salt is a potent antibiotic and belongs to the carbapenem class of antibiotics.
It is effective against a broad spectrum of Gram-positive and Gram-negative bacteria, including multidrug-resistant strains.
In the field of microbiology and infectious disease research, Ertapenem Sodium Salt is commonly used as a tool for studying bacterial susceptibility and resistance. It can be employed in antimicrobial susceptibility testing to determine the efficacy of different antibiotics against bacterial isolates.
Medchemexpress LLC Thioacetamide | 62-55-5 | MFCD00008070 | 98.0% | 75.13 g/mol | C2H5NS | 1g
Thioacetamide (TAA) is an indirect hepatotoxin and causes parenchymal cell necrosis Thioacetamide requires metabolic activation by microsomal CYP2E1 to thioacetamide-S-oxide initially and then to thioacetamide-S-dioxide which is a highly reactive metabolite and its reactive metabolites covalently bind to proteins and lipids thereby causing oxidative stress and centrilobular necrosis Thioacetamide can induce chronic liver fibrosis encephalopathy and other events model[1][2][3][4]
Medchemexpress LLC Sulfanilamide | 63-74-1 | 99.93% | 5 G
Sulfanilamide (Sulphanilamide) is a potent and orally active sulfonamide antibiotic and can be a major intermediate of sulfamethoxazole biodegradation. It is also a carbonic anhydrase inhibitor and shows inhibition on the virus of lymphogranuloma venereum.
- Potent and orally active sulfonamide antibiotic
- Major intermediate of sulfamethoxazole biodegradation
- Carbonic anhydrase inhibitor
- Shows inhibition on the virus of lymphogranuloma venereum
Sigma Aldrich Fine Chemicals Biosciences 4-(Methylthio)butanol 97%, FG | 20582-85-8 | MFCD00002973 |
4-(Methylthio)butanol 97%, FG | Purity: 97% | Mol Wt: 120.21 | 20582-85-8 | MFCD00002973 |
Medchemexpress LLC Diphenyl disulfide | 882-33-7 | MFCD00003065 | 100.0% | 218.35 g/mol | C12H10S2 | 1g
Diphenyl disulfide is an endogenous metabolite Diphenyl disulfide is a pharmaceutical intermediate Diphenyl disulfide can be coupled with aryl iodide to synthesize asymmetric aryl sulfide[1][2]
Medchemexpress LLC Sulfanilamide | 63-74-1 | 99.3% | 1 G
Sulfanilamide is a potent and orally active sulfonamide antibiotic, also serving as a major intermediate in sulfamethoxazole biodegradation. This compound acts as a carbonic anhydrase inhibitor and has demonstrated inhibition against the virus of lymphogranuloma venereum. It presents as a white to off-white solid and is intended solely for research and analytical applications.
- Potent and orally active sulfonamide antibiotic properties
- Functions as a carbonic anhydrase inhibitor
- Exhibits inhibition against the virus of lymphogranuloma venereum
- Store powder at -20°C for up to 3 years, or 4°C for up to 2 years
- Store in solvent at -80°C for up to 2 years, or -20°C for up to 1 year
AdipoGen PJ-34
Chemical. CAS 344458-15-7. Formula C17H17N3O2 . HCl. MW 295.2 . 36.5. Potent, water soluble polyADP-ribose polymerase PARP inhibitor. Inhibits peroxynitrite-induced cell necrosis. Shows significant, dose-dependent anti-inflammatory effects in a variety of local inflammation models. Provides cardioprotection by decreasing myocardial infarct size. Shows protective effects in models of stroke. Suppresses cell growth in liver cancer cells.
Selleck Chemical LLC ZEN-3694-E1517-1G
ZEN-3694 is an orally bioavailable bromodomain extraterminal inhibitor (BETi) that leads to down-regulation of expression of AR-signaling in metastatic castrationresistant prostate cancer (mCRPC) models