25945-95-3

Upstream product

• 121-88-0 5-Nitro-2-aminophenol 
• 25945-96-4 2-benzyloxy-4-nitro-phenylamine 
• 75-36-5 acetyl chloride 
• 25351-89-7 N-(2-hydroxy-4-nitrophenyl)acetamide 
• 100-44-7 benzyl chloride 

Downstream Products

• 106994-23-4 N-(4-Allylamino-3,6-dioxo-cyclohexa-1,4-dienyl)-acetamide 
• 106994-11-0 2-acetamido-5--4-diazocyclohexadien-1-one 
• 116911-66-1 1-(phenylsulfonyl)-7-(benzyloxy)-3-methyl-4,6-dinitro-5-indole 
• 116911-69-4 1-(phenylsulfonyl)-7-<(ethoxycarbonyl)oxy>-4-nitro-5-indole 
• 116911-65-0 1-(phenylsulfonyl)-7-(benzyloxy)-3-methyl-4-nitro-5-indole 
• 116911-67-2 1-(phenylsulfonyl)-7-hydroxy-3-methyl-4-nitro-5-indole 
• 116911-70-7 1-(phenylsulfonyl)-4-diazo-3-methyl-5--4,7-dihydroindol-7-one 
• 116911-77-4 C₁₉H₁₈N₂O₅S₂ 
• 116911-78-5 Methanesulfinic acid allyl-(1-benzenesulfonyl-3-methyl-4,7-dioxo-4,7-dihydro-1H-indol-5-yl)-amide 
• 116911-62-7 7-(benzyloxy)-3-methyl-5-indole 
• 116911-60-5 N-<4-acetamido-3-(benzyloxy)phenyl>-N-(2-propenyl)-methanesulfonamide 
• 116911-76-3 5-Allylamino-1-benzenesulfonyl-3-methyl-1H-indole-4,7-dione 
• 116911-61-6 N-<4-amino-3-(benzyloxy)phenyl>-N-(2-propenyl)-methanosulfonamide 
• 106994-14-3 N-<4-acetamido-5-(benzyloxy)-2-nitrophenyl>-N-(2-propenyl)methanesulfonamide 

Relevant academic research and scientific papers

Novel sulfonanilide analogs decrease aromatase activity in breast cancer cells: Synthesis, biological evaluation, and ligand-based pharmacophore identification

Aromatase converts androgens to estrogens and is a particularly attractive target in the treatment of estrogen receptor positive breast cancer. Previously, the COX-2 selective inhibitor nimesulide and analogs decreased aromatase expression and enzyme acti

SULFONANILIDE ANALOGS AS SELECTIVE AROMATASE MODULATORS

Compounds and methods suppressing aromatase activity expression in cancer cells. Provided are compounds are those of formula I: wherein R1 may be alkyl, cycloakyl, haloalkyl, aryl, substituted aryl, haloaryl, alkoxy, alkylaryl, and arylalkyl; R2 is H, alk

PHOTOCHEMISTRY OF QUINONE DIAZIDES. INTRAMOLECULAR OXYGEN TRANSFER AND CARBENOID ADDITION DURING PHOTOLYSIS OF N-ALLYLSULFONAMIDO QUINONE DIAZIDES

An indole quinone diazide, 5-(N-allylsulfonamido)-4-diazo-3-methyl-4,7-dihydroindol-7-one, which is a potential precursor of a spiro-cyclopropane-indol-7-one structure has been prepared.A study of its photolysis and that of a model compound has identified oxygen transfer from the sulfonamido substituent as a process which competes with intramolecular carbenoid addition.