Sulfonyls
Sigma Aldrich N-Methyl-1-(3-pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanamine trifluoroacetate
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich Trifluoromethanesulfonimide
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich Sulfanilamide
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
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
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
eMolecules 421-83-0 | AstaTech | TRIFLUOROMETHANESULFONYL CHLORIDE | 1g | 718085466 | D92440 | 95 | MFCD00007451 | 168.51 | CClF3O2S
AstaTech | 1-PYRENEMETHYLAMINE HYDROCHLORIDE | 0.1g | 718066307 | E78136 | 95.000 | 93324-65-3 | MFCD00192425 | 267.760 | C17H14ClN
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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% | 1 ML
Sulfapyridine is a sulfonamide antibiotic agent and a major metabolite of Sulfasalazine. It inhibits recombinant P. carinii dihydropteroate synthetase (DHPS) with an IC50 of 0.18 μM. It exhibits antibacterial, anti-inflammatory, and anti-rheumatic activities.
- Inhibits recombinant P. carinii dihydropteroate synthetase (DHPS)
- Exhibits antibacterial properties
- Possesses anti-inflammatory activity
- Shows anti-rheumatic activity
- Inhibits production of IL-8, CXCL1, and MCP-1 in synovial cells of rheumatoid arthritis (RA)
- Significantly inhibits systemic allergic reactions induced by compound 48/80 in rats
Medchemexpress LLC Sulfanilamide | 63-74-1 | MFCD00007939 | 99.9% | 10 MM IN 1 ML
Sulfanilamide is a potent and orally active sulfonamide antibiotic. It is a major intermediate of sulfamethoxazole biodegradation. It also functions as a carbonic anhydrase inhibitor and exhibits inhibition against the virus of lymphogranuloma venereum.
- Potent anti-infection activity in albino mice
- Inhibits HepG2 cells with an IC50 of 0.08 μM
- Inhibits K562 cells with an IC50 of 0.2 μM
- Inhibits MDA-MB-231 cells with an IC50 of 0.09 μM
ALADDIN SCIENTIFIC CORPORATION Sulfanilamide, 100g
Sulfonamide antibacterial Sulfanilamide is an antibacterial and used in the treatment of vaginal yeast infections It is a competitive inhibitor of dihydropteroate synthestase to block the synthesis of folic acid It serves as an intermediate for the preparation of 26-disubstituted anilines by electrophilic substitution followed by removal of the sulfonamide blocking group by desulfonation with sulfuric acid
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.
Matrix Scientific 2- N,N-BIS(TRIFLUOROMETHANE-1G
2-[N,N-Bis(trifluoromethanesulfonyl)amino]-5-chloropyridine, 99%; 1g,C7H3ClF6N2O4S2, MFCD00191833, mw 392.68, [145100-51-2]