97986-02-2

Basic information

• Product Name: L-Alaninamide, N-[(phenylmethoxy)carbonyl]glycyl-L-alanyl-N-(4-nitrophenyl)-
• CAS NO: 97986-02-2
• Molecular Formula: C22H25N5O7
• Molecular Weight: 471.47
• Mol File: 97986-02-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: L-Alaninamide, N-[(phenylmethoxy)carbonyl]glycyl-L-alanyl-N-(4-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: L-Alaninamide, N-[(phenylmethoxy)carbonyl]glycyl-L-alanyl-N-(4-nitrophenyl)-(97986-02-2)
• EPA Substance Registry System: L-Alaninamide, N-[(phenylmethoxy)carbonyl]glycyl-L-alanyl-N-(4-nitrophenyl)-(97986-02-2)

Safety Data

• Hazardous Substances Data: 97986-02-2(Hazardous Substances Data)

Upstream product

• 16816-28-7 methyl 2-[({[(benzyloxy)carbonyl]amino}acetyl)amino]propanoate 
• 23404-17-3 benzyloxycarbonylglycyl-alanine hydrazide 
• 1668-13-9 L-alanine-p-nitroanilide 

Downstream Products

• 85589-15-7 3-carboxypropionylglycyl-alanyl-alanine p-nitroanilide 

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.