Organosulfur Compounds
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 Sulfathiazole (sodium) | 144-74-1 | 99.9% | 1 G
Sulfathiazole (sodium) | 144-74-1 | 99.9% | 1 G
Sigma Aldrich Fine Chemicals Biosciences Sulfanilamide European Pharmacopoeia (EP) Reference Standard | 63-74-1 | MFCD00007939 |
Sulfanilamide European Pharmacopoeia (EP) Reference Standard | Mol Wt: 172.2 | 63-74-1 | MFCD00007939 |
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 | 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 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