Sulfonyls
Medchemexpress LLC Sulfadiazine (standard) | 68-35-9 | 99.8% | 50 MG
Sulfadiazine (Standard) is the analytical standard of Sulfadiazine. This product is intended for research and analytical applications. Sulfadiazine is a sulfonamide antibiotic with antimalarial activity and can be used for toxoplasmosis research.
- It serves as an analytical standard.
- Intended for research and analytical applications.
- Possesses sulfonamide antibiotic properties.
- Demonstrates antimalarial activity.
- Suitable for toxoplasmosis research.
- Can be used in qualitative, quantitative, and methodological research experiments.
- Applicable in techniques such as HPLC, GC, and MS.
eMolecules 5934-14-5 | 4-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid | 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 Sulfathiazole (sodium) | 144-74-1 | 99.9% | 1 ML
Sulfathiazole sodium is an analytical standard suitable for research and analytical applications such as HPLC, GC, and MS. It acts as an orally active endocrine disruptor, notably enhancing CYP19 activity in human adrenal cancer cells (H295R) and upregulating the mRNA expression of CYP17, CYP19, and 3β-HSD. The compound also increases 17-estradiol (E2) production and exhibits endocrine disrupting effects on aquatic organisms. Furthermore, it functions as a cathodic corrosion inhibitor by reducing corrosion current density and shifting corrosion potential negatively.
- Enhances CYP19 activity in human adrenal cancer cells
- Upregulates mRNA expression of CYP17, CYP19, and 3β-HSD
- Increases 17-estradiol (E2) production
- Exhibits endocrine disrupting effects on aquatic organisms
- Inhibits copper corrosion by chloride ions
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
Medchemexpress LLC Sulfapyridine | 144-83-2 | 99.9% | 250 MG
Sulfapyridine (Standard) is an analytical standard intended for research and analytical applications. As a sulfonamide antibiotic agent and a major metabolite of Sulfasalazine, it demonstrates antibacterial, anti-inflammatory, and anti-rheumatic activities. It is also noted for its ability to inhibit recombinant *P. carinii* dihydropteroate synthetase (DHPS) with an IC50 of 0.18 μM.
- Analytical standard for research and analytical applications
- Reference standard for assay supply
- Used in qualitative, quantitative, and methodological research experiments (HPLC, GC, MS)
- Functions as a sulfonamide antibiotic agent
- Exhibits antibacterial, anti-inflammatory, and anti-rheumatic activities
- Inhibits *P. carinii* dihydropteroate synthetase (DHPS)
Revvity Health Sciences Inc HTRF Human CD47 / SIRP-α Binding Kit, 10,000 Assay Points
HTRF Human CD47 / SIRP-α Binding Kit, 10,000 Assay Points
Medchemexpress LLC Sulfathiazole | 72-14-0 | 99.7% | 10 G
Sulfathiazole is an orally active endocrine disruptor that targets the steroidogenic pathway. It enhances the activity of CYP19 in human adrenal cancer cells (H295R) and has endocrine-disrupting effects on aquatic organisms.
- Enhances CYP19 activity in human adrenal cancer cells (H295R).
- Upregulates mRNA expression of CYP17, CYP19, and 3β-HSD.
- Increases production of 17-estradiol (E2).
- Exhibits endocrine-disrupting effects on aquatic organisms like the Japanese medaka fish.
- For research use only.
Medchemexpress LLC Sulfathiazole | 72-14-0 | 99.7% | 1 ML
Sulfathiazole is an orally active endocrine disruptor that targets the steroidogenic pathway. It enhances CYP19 activity in human adrenal cancer cells and upregulates the mRNA expression of CYP17, CYP19, and 3β-HSD. This compound increases 17-estradiol (E2) production and exhibits endocrine disrupting effects on aquatic organisms.
- Orally active endocrine disruptor
- Targets the steroidogenic pathway
- Enhances CYP19 activity in human adrenal cancer cells
- Upregulates mRNA expression of CYP17, CYP19, and 3β-HSD
- Increases 17-estradiol (E2) production
- Exhibits endocrine disrupting effects on aquatic organisms
- Shows antibacterial properties
- Effective in inhibiting copper corrosion in 0.1 M NaCl solution
Medchemexpress LLC Sulfathiazole (sodium) | 144-74-1 | 99.9% | 1 G
Sulfathiazole (sodium) | 144-74-1 | 99.9% | 1 G
Medchemexpress LLC Sulfathiazole | 72-14-0 | 99.7% | 5 G
Sulfathiazole is an orally active compound identified as an endocrine disruptor. It specifically targets the steroidogenic pathway by enhancing the activity of CYP19 in human adrenal cancer cells (H295R) and increasing the mRNA expression of CYP17, CYP19, and 3β-HSD. This leads to an increased production of 17-estradiol (E2) and has been observed to cause endocrine disrupting effects on aquatic organisms such as the Japanese medaka fish.
- Orally active.
- Targets the steroidogenic pathway.
- Enhances CYP19 activity in human adrenal cancer cells (H295R).
- Upregulates mRNA expression of CYP17, CYP19, and 3β-HSD.
- Increases 17-estradiol (E2) production.
- Exhibits endocrine disrupting effects on aquatic organisms (e.g., Japanese medaka fish).
- Can inhibit the corrosion of copper in 0.1 M NaCl solution, with efficiency exceeding 80% at increased concentrations.
Apexbio Technology LLC Sulfanilamide 63-74-1 10mM (in 1mL DMSO)
Sulfanilamide is a competitive inhibitor targeting bacterial dihydropteroate synthetase (DHPS) an enzyme essential in microbial folate biosynthesis pathway By inhibiting DHPS the compound limits synthesis of dihydrofolate a precursor crucial for bacterial DNA replication and proliferation In enzymatic assays evaluating inhibition potency Sulfanilamide demonstrates an IC50 value of approximately 320 M Due to its defined mode of action Sulfanilamide is extensively utilized in microbiology and pharmacology research particularly for investigating bacterial metabolic pathways resistance mechanisms and screening potential antibacterial agents