80852-51-3

Upstream product

• 93-11-8 2-Naphthalenesulfonyl chloride 
• 52117-01-8 N-acetyl-4-cyano-α-(ethoxycarbonyl)phenylalanine ethyl ester 
• 80852-46-6 Nα-(2-Naphthylsulfonyl)-4-cyanphenylalanin 
• 80852-40-0 Nα-(2-Naphthylsulfonyl)-4-carbamoylphenylalanin 

Downstream Products

• 80852-86-4 N_α-2-Naphtylsulfonyl-4-cyanphenylalanin-4-methylpiperidid 
• 83973-05-1 3-(4-Cyano-phenyl)-2-(naphthalene-2-sulfonylamino)-propionic acid octyl ester 
• 80840-58-0 Nα-(2-Naphthylsulfonyl)-4-amidinophenylalanin-4'-methylpiperididhydroiodid 
• 80840-60-4 3-(4-Carbamimidoyl-phenyl)-N-cyclohexyl-2-(naphthalene-2-sulfonylamino)-propionamide; hydriodide 
• 75077-37-1 4-[3-Morpholin-4-yl-2-(naphthalene-2-sulfonylamino)-3-oxo-propyl]-benzamidine; hydriodide 
• 71078-90-5 4-[2-(Naphthalene-2-sulfonylamino)-3-oxo-3-piperidin-1-yl-propyl]-benzamidine; hydriodide 
• 80840-61-5 N-Benzyl-3-(4-carbamimidoyl-phenyl)-2-(naphthalene-2-sulfonylamino)-propionamide; hydriodide 
• 80840-59-1 N-Butyl-3-(4-carbamimidoyl-phenyl)-2-(naphthalene-2-sulfonylamino)-propionamide; hydriodide 
• 71078-91-6 4-[2-(Naphthalene-2-sulfonylamino)-3-oxo-3-pyrrolidin-1-yl-propyl]-benzamidine; hydriodide 
• 88910-13-8 α-(2-Naphthylsulfonylamino)-β-(4-amidinophenyl)ethyl-chlormethylketonacetat 
• 80853-59-4 4-[2-Cyclohexylcarbamoyl-2-(naphthalene-2-sulfonylamino)-ethyl]-thiobenzimidic acid methyl ester; hydriodide 
• 88910-09-2 Thioimidsaeuremethylesterhydroiodid 
• 80853-25-4 N-Cyclohexyl-2-(naphthalene-2-sulfonylamino)-3-(4-thiocarbamoyl-phenyl)-propionamide 
• 118964-62-8 1-[3-(4-Methylsulfanylcarbonimidoyl-phenyl)-2-(naphthalene-2-sulfonylamino)-propionyl]-pyrrolidine-2-carboxylic acid; hydriodide 

Relevant academic research and scientific papers

Synthetic serine protease inhibitors. 29. Synthesis of alpha-arylsulphonylamino-beta-(4-amidinophenyl)ethyl-chloromethylketones and their inhibitory activity against trypsin, plasmin and thrombin

The synthesis of alpha-arylsulphonylamino-beta-(4-amidinophenyl)ethyl-chloromethylketones, the structures of which correspond largely to those of the antiproteolytically very potent N alpha-arylsulphonylated 4-amidinophenylalaninamides, was realized start