85589-16-8

Basic information

• Product Name: 3-carboxypropionylalanyl-glycyl-alanine p-nitroanilide
• CAS NO: 85589-16-8
• Molecular Weight: 437.409
• Mol File: 85589-16-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-carboxypropionylalanyl-glycyl-alanine p-nitroanilide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-carboxypropionylalanyl-glycyl-alanine p-nitroanilide(85589-16-8)
• EPA Substance Registry System: 3-carboxypropionylalanyl-glycyl-alanine p-nitroanilide(85589-16-8)

Safety Data

• Hazardous Substances Data: 85589-16-8(Hazardous Substances Data)

Upstream product

• 108-30-5 succinic acid anhydride 
• 2503-32-4 ethyl N-(benzyloxycarbonyl)-L-alanylglycinate 
• 111195-97-2 [(S)-1-({[(S)-1-(4-Nitro-phenylcarbamoyl)-ethylcarbamoyl]-methyl}-carbamoyl)-ethyl]-carbamic acid benzyl ester 
• 58651-28-8 benzyloxycarbonylalanyl-glycine hydrazide 

Relevant articles and documents

ROLE OF AMINO ACID RESIDUES IN CHROMOGENIC SUBSTRATES CLEAVED BY PANCREATIC ELASTASE

Anionic chromogenic substrates, 3-carboxypropionyl tripeptide p-nitroanilides modified with glycine, β-alanine, alanine, leucine, and proline in positions P1, P2, and P3 were synthesized.The substrates were digested with pancreatic elastase and the values of Km, kcat, and kcat/Km were determined.Alanine plays a decisive role in position P1, substrates with glycine or β-alanine in this position are not cleaved.The substitution in P2 is dominant for proline; next follow alanine, leucine, and glycine.The substitution in P3 is the least specific one.