Sulfonyls
Sulfapyridine, ≥99.0%, MilliporeSigma™ Supelco™
MDL Number: MFCD00038036 Synonym: 4-Amino-N-[2-pyridyl]benzene sulfonamide; N1-(Pyridin-2-yl)sulfanilamide
Sulfapyridine, British Pharmacopoeia (BP) Reference Standard, MilliporeSigma™ Supelco™
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets, has been developed and issued under the Authority of the issuing Pharmacopoeia.
Sulfanilamide Reagent (1% w/v) in 10% v/v Hydrochloric Acid, Reagents
CAS: 7732-18-5 Molecular Formula: H2O Molecular Weight (g/mol): 18.02 InChI Key: XLYOFNOQVPJJNP-UHFFFAOYSA-N Synonym: Sulfamine, 4-Aminobenzenesulfonamide IUPAC Name: water SMILES: O
Sulfanilamide, 98%
CAS: 63-74-1 Molecular Formula: C6H8N2O2S Molecular Weight (g/mol): 172.202 MDL Number: MFCD00007939 InChI Key: FDDDEECHVMSUSB-UHFFFAOYSA-N Synonym: sulfanilamide,sulphanilamide,sulfamine,sulphonamide,p-aminobenzenesulfonamide,sulfonylamide,sulfonamide,p-aminobenzenesulfamide,bacteramid,streptasol PubChem CID: 5333 ChEBI: CHEBI:45373 IUPAC Name: 4-aminobenzenesulfonamide SMILES: C1=CC(=CC=C1N)S(=O)(=O)N
Sulfathiazole, 98+%
CAS: 72-14-0 Molecular Formula: C9H9N3O2S2 Molecular Weight (g/mol): 255.31 MDL Number: MFCD00005319 InChI Key: JNMRHUJNCSQMMB-UHFFFAOYSA-N Synonym: sulfathiazole,sulphathiazole,sulfathiazol,sulfanilamidothiazole,2-sulfanilamidothiazole,norsulfazole,thiazamide,2-sulfonamidothiazole,norsulfasol,neostrepsan PubChem CID: 5340 ChEBI: CHEBI:9337 IUPAC Name: 4-amino-N-(1,3-thiazol-2-yl)benzenesulfonamide SMILES: NC1=CC=C(C=C1)S(=O)(=O)NC1=NC=CS1
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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eMolecules 41513-78-4 | Ambeed | 2-(13-Dioxoisoindolin-2-yl)benzoic acid | 1g | 573005493 | A869899 | MFCD00041218 | 267.24 | C15H9NO4
Ambeed | 2-Bromo-1-(33-dinitroazetidin-1-yl)ethan-1-one | 5mg | 534568145 | A400874 | 925206-65-1 | MFCD25976849 | 268.023 | C5H6BrN3O5
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eMolecules 40732-91-0 | 4-(1,3-Dioxoisoindolin-2-yl)-2-hydroxybutanoic acid | Ambeed | MFCD01457304 | 249.222 | C12H11NO5 | 97.000 | OC(CCN1C(=O)c2ccccc2C1=O)C(O)=O | 5g | 601097039
4-(1,3-Dioxoisoindolin-2-yl)-2-hydroxybutanoic acid | Ambeed | 40732-91-0 | MFCD01457304 | 249.222 | C12H11NO5 | 97.000 | OC(CCN1C(=O)c2ccccc2C1=O)C(O)=O | 5g | 601097039
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
Apexbio Technology LLC Sulfadiazine 68-35-9 5g
Sulfadiazine (CAS 68-35-9) is a small-molecule inhibitor targeting dihydropteroate synthase It is designed to inhibit microbial folate biosynthesis thereby disrupting folic acid synthesis required for pathogen proliferation Sulfadiazine exerts its biological activity primarily through the competitive inhibition of dihydropteroate synthase In in vitro studies Sulfadiazine demonstrates antiparasitic activity with IC50 values ranging from approximately 2 g/mL to 5 g/mL against Toxoplasma gondii depending on experimental conditions and parasite strains Based on these pharmacological properties Sulfadiazine holds research potential in antiparasitic activity evaluation and studies of folic acid metabolism pathways
Apexbio Technology LLC Sulfapyridine 144-83-2 5g
Sulfapyridine (144-83-2) is a small-molecule inhibitor targeting bacterial dihydropteroate synthase It functions by inhibiting this enzyme thus blocking folic acid synthesis and suppressing bacterial growth Sulfapyridine exerts its biological activity primarily through inhibition of bacterial dihydropteroate synthase In in vitro studies sulfapyridine demonstrates inhibitory activity with IC50 values typically ranging from approximately 5 g/mL to 20 g/mL depending on the bacterial strain and assay conditions Based on these pharmacological properties sulfapyridine holds research potential in antimicrobial susceptibility testing investigations of bacterial resistance mechanisms and studies of bacterial folate pathway enzymes
Apexbio Technology LLC Sulfathiazole 72-14-0 10g
Sulfathiazole (CAS 72-14-0) is a small-molecule inhibitor targeting dihydropteroate synthase (DHPS) It is designed to competitively inhibit bacterial folic acid synthesis thereby disrupting the folate pathway and impeding microbial growth Sulfathiazole exerts its biological activity primarily through inhibition of DHPS In in vitro studies sulfathiazole demonstrates bacteriostatic inhibition with IC50 values ranging from low to medium micromolar concentrations depending on specific bacterial strains and experimental conditions Based on these pharmacological properties sulfathiazole holds research potential in investigating antibacterial resistance metabolic pathways of pathogens and enzyme-substrate interactions in microbiological and biochemical research
Apexbio Technology LLC Sulfathiazole 72-14-0 10mM (in 1mL DMSO)
Sulfathiazole (CAS 72-14-0) is a small-molecule inhibitor targeting dihydropteroate synthase (DHPS) It is designed to competitively inhibit bacterial folic acid synthesis thereby disrupting the folate pathway and impeding microbial growth Sulfathiazole exerts its biological activity primarily through inhibition of DHPS In in vitro studies sulfathiazole demonstrates bacteriostatic inhibition with IC50 values ranging from low to medium micromolar concentrations depending on specific bacterial strains and experimental conditions Based on these pharmacological properties sulfathiazole holds research potential in investigating antibacterial resistance metabolic pathways of pathogens and enzyme-substrate interactions in microbiological and biochemical research