134303-72-3

Basic information

• Product Name: Z-Gly-Pro-Arg(NO₂)-Pro-OBzl
• CAS NO: 134303-72-3
• Molecular Weight: 694.745
• Mol File: 134303-72-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Z-Gly-Pro-Arg(NO₂)-Pro-OBzl(CAS DataBase Reference)
• NIST Chemistry Reference: Z-Gly-Pro-Arg(NO₂)-Pro-OBzl(134303-72-3)
• EPA Substance Registry System: Z-Gly-Pro-Arg(NO₂)-Pro-OBzl(134303-72-3)

Safety Data

• Hazardous Substances Data: 134303-72-3(Hazardous Substances Data)

Upstream product

• 134303-57-4 Boc-Pro-Arg(NO₂)-Pro-OBzl 
• 54046-53-6 Boc-Arg(NO₂)-Pro-OBzl 
• 85918-68-9 H-Arg(NO₂)-Pro-OBzl 
• 2188-18-3 N-alpha-t-butoxycarbonyl-Ng-nitroarginine 
• 16652-71-4 benzyl (2S)-2-pyrrolidinecarboxylate hydrochloride 
• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 
• 41324-66-7 H-Pro-OBzl 
• 148205-61-2 Z(OMe)-Arg(NO₂)-Pro-OBzl 
• 57294-41-4 Z-Gly-Pro-OBzl 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 
• 23234-71-1 Z(OMe)-Arg(NO₂)-OH 
• 838819-77-5 H-Pro-Arg(NO₂)-Pro-OBzl 
• 23828-53-7 Z-Gly-Pro-NHNH₂ 

Downstream Products

• 67869-62-9 Gly-Pro-Arg-Pro 

Relevant articles and documents

Amino acids and peptides. XVI. Synthesis of N-terminal tetrapeptide analogs of fibrin α-chain and their inhibitory effects on fibrinogen/thrombin clotting

N-Terminal tetrapeptide analogs of fibrin α-chain were synthesized by the solution method using a new active ester, the ester of the oxime of p-nitroacetophenone, and by the solid-phase method. Their inhibitory effects on fibrinogen/thrombin clotting were examined. Of the synthetic peptides, amide analogs of Gly-Pro-Arg-Pro exhibited a more potent inhibitory effect.