Sulfonyls
eMolecules 4-Amino-N-(pyrimidin-2-yl)benzene-1-sulfonamide | Combi-Blocks | 68-35-9 | MFCD00006065 | 250.280 | C10H10N4O2S | 98.000 | Nc1ccc(cc1)S(=O)(=O)Nc1ncccn1 | 5g | 296391758
4-Amino-N-(pyrimidin-2-yl)benzene-1-sulfonamide | Combi-Blocks | 68-35-9 | MFCD00006065 | 250.280 | C10H10N4O2S | 98.000 | Nc1ccc(cc1)S(=O)(=O)Nc1ncccn1 | 5g | 296391758
Apexbio Technology LLC Sulfanilamide 63-74-1 50g
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 Ambeed / 4-(13-Dioxoisoindolin-2-yl)-2-hydroxybutanoic acid / 5g / 601097039 / A252457 / / 40732-91-0 / MFCD01457304 / 249.222 / C12H11NO5
Ambeed / 4-(13-Dioxoisoindolin-2-yl)-2-hydroxybutanoic acid / 5g / 601097039 / A252457 / / 40732-91-0 / MFCD01457304 / 249.222 / C12H11NO5
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
eMolecules Pharmablock / 2-cyclohexyl-2-(13-dioxoisoindolin-2-yl)acetic acid / 25mg / 586143202 / PBA0014 / 0.000 / 1218299-30-9 / MFCD18477507 / 287.315 / C16H17NO4
Pharmablock / 2-cyclohexyl-2-(13-dioxoisoindolin-2-yl)acetic acid / 25mg / 586143202 / PBA0014 / 0.000 / 1218299-30-9 / MFCD18477507 / 287.315 / C16H17NO4
eMolecules Ambeed / 2-(13-Dioxoisoindolin-2-yl)benzoic acid / 1g / 573005493 / A869899 / / 41513-78-4 / MFCD00041218 / 267.240 / C15H9NO4
Ambeed / 2-(13-Dioxoisoindolin-2-yl)benzoic acid / 1g / 573005493 / A869899 / / 41513-78-4 / MFCD00041218 / 267.240 / C15H9NO4
Revvity Health Sciences Inc HTRF Human CD47 / SIRP-α Binding Kit, 500 Assay Points
HTRF Human CD47 / SIRP-α Binding Kit, 500 Assay Points
Sulfabenzamide, 100.1%, MP Biomedicals™
CAS: 127-71-9 Molecular Formula: C13H12N2O3S Molecular Weight (g/mol): 276.31 InChI Key: PBCZLFBEBARBBI-UHFFFAOYSA-N Synonym: sulfabenzamide,sulfabenzide,sulfabenzid,sulfabenzoylamide,n-sulfanilylbenzamide,n-sulfamylbenzamide,n-benzoylsulfanilamide,sulfamylbenzamide,sulfabenzamid,sulfabenzamida PubChem CID: 5319 IUPAC Name: N-(4-aminophenyl)sulfonylbenzamide SMILES: C1=CC=C(C=C1)C(=O)NS(=O)(=O)C2=CC=C(C=C2)N
3-Amino-4-chloro-N-(2-cyanoethyl)benzenesulfonamide 98%, Thermo Scientific™
CAS: 64415-13-0 Molecular Formula: C9H10ClN3O2S Molecular Weight (g/mol): 259.708 InChI Key: DNMYCTLTLUHRRT-UHFFFAOYSA-N PubChem CID: 97449 IUPAC Name: 3-amino-4-chloro-N-(2-cyanoethyl)benzenesulfonamide SMILES: C1=CC(=C(C=C1S(=O)(=O)NCCC#N)N)Cl