909124-91-0

Upstream product

• 98-60-2 4-chlorobenzenesulfonyl chloride 
• 367-30-6 2,5-difluoroaniline 
• 619-14-7 3-hydroxy-4-nitro-benzoic acid 
• 909124-87-4 [3-(3-bromo-propoxy)-4-(1-hydroxy-ethyl)-phenyl]-[4-(tert-butyl-dimethyl-silanyloxymethyl)-phenyl]-methanone 
• 909124-68-1 3-(3-bromo-propoxy)-N-methoxy-N-methyl-4-trimethylsilanylethynyl-benzamide 
• 909124-71-6 3-(3-bromo-propoxy)-4-(1-hydroxy-ethyl)-N-methoxy-N-methyl-benzamide 
• 909124-69-2 4-acetyl-3-(3-bromo-propoxy)-N-methoxy-N-methyl-benzamide 
• 909124-66-9 3-hydroxy-N-methoxy-N-methyl-4-trimethylsilanylethynyl-benzamide 
• 909124-60-3 3-hydroxy-N-methoxy-N-methyl-4-nitro-benzamide 
• 909124-62-5 4-amino-3-hydroxy-N-methoxy-N-methyl-benzamide 
• 909124-64-7 3-hydroxy-4-iodo-N-methoxy-N-methyl-benzamide 
• 290331-05-4 4-chloro-N-[5-fluoro-2-fluorophenyl]benzenesulfonamide 
• 909124-89-6 N-(1-{2-(3-bromo-propoxy)-4-[4-(tert-butyl-dimethyl-silanyloxymethyl)-benzoyl]-phenyl}-ethyl)-4-chloro-N-(2,5-difluoro-phenyl)-benzenesulfonamide 

Relevant academic research and scientific papers

Synthesis of biotinylated photoaffinity probes based on arylsulfonamide γ-secretase inhibitors

Synthesis and biological evaluation of an arylsulfonamide class of γ-secretase inhibitors are described. Design, synthesis, and biological evaluation of multifunctional molecular probes harboring a benzophenone photophore as a cross-linking group and a biotin tag are also reported.