202411-01-6

Basic information

• Product Name: Boc-Arg(Tos)-Pro-Ala-Lys(Z)-OBzl
• Synonyms: Boc-Arg(Tos)-Pro-Ala-Lys(Z)-OBzl
• CAS NO: 202411-01-6
• Molecular Weight: 949.138
• Mol File: 202411-01-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Boc-Arg(Tos)-Pro-Ala-Lys(Z)-OBzl(CAS DataBase Reference)
• NIST Chemistry Reference: Boc-Arg(Tos)-Pro-Ala-Lys(Z)-OBzl(202411-01-6)
• EPA Substance Registry System: Boc-Arg(Tos)-Pro-Ala-Lys(Z)-OBzl(202411-01-6)

Safety Data

• Hazardous Substances Data: 202411-01-6(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 68641-29-2 N^α-Boc-Pro-OBt 
• 13836-37-8 Boc-Arg(Tos)-OH 
• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 
• 202410-99-9 Boc-Pro-Ala-Lys(Z)-OBzl 
• 77236-13-6 N-α-tert-Butyloxycarbonyl-N-ε-carbobenzoxy-L-lysine benzyl ester 
• 114856-02-9 Boc-Ala-Lys(Z)-OBzl 
• 6366-70-7 N^ε-carbobenzoxy-L-lysine benzyl ester hydrochloride 
• 2389-45-9 Boc-Lys(Z)-OH 
• 105916-77-6 N^α-Boc-N^δ-tosyl-Arg-OBt 

Downstream Products

• 860020-54-8 N-[1-(1',3'-dioxyl-4',4',5',5'-tetramethyldihydroimidazol-2-yl)phenyl-4-yl]oxyacetyl-Gly-Arg(Tos)-Pro-Ala-Lys(Z)-OBzl 
• 860020-53-7 N-[1-(1',3'-dioxyl-4',4',5',5'-tetramethyldihydroimidazol-2-yl)phenyl-4-yl]oxyacetyl-Ala-Arg(Tos)-Pro-Ala-Lys(Z)-OBzl 
• 860020-55-9 N-[1-(1',3'-dioxyl-4',4',5',5'-tetramethyldihydroimidazol-2-yl)phenyl-4-yl]oxyacetyl-Gln-Arg(Tos)-Pro-Ala-Lys(Z)-OBzl 
• 202411-03-8 Boc-Ala-Arg(Tos)-Pro-Ala-Lys(Z)-OBzl 
• 202411-04-9 Boc-Gln-Arg(Tos)-Pro-Ala-Lys(Z)-OBzl 
• 544477-17-0 Boc-Gly-Arg(Tos)-Pro-Ala-Lys(Z)-OBzl 
• 202411-08-3 Boc-Gln-Arg(Tos)-Pro-Ala-Lys(Z)-OH 
• 202411-07-2 Boc-Ala-Arg(Tos)-Pro-Ala-Lys(Z)-OH 

Relevant articles and documents

A new class of β-carboline alkaloid-peptide conjugates with therapeutic efficacy in acute limb ischemia/reperfusion injury

We describe a novel class of β-carboline alkaloid-peptide conjugates that possess both free radical scavenging and thrombolytic activity. These conjugates demonstrate therapeutic efficacy in a rat arterial thrombosis assay, as well as free radical scavenging capacity as evaluated in a PC12 cell survival assay. Our results indicate that β-carboline alkaloid-peptide conjugate 26a exerts a significant protective effect against local and remote organ injury induced by limb I/R injury in the rat.

Studies on Hybrid Peptides of Fragments from Fibrinogen

In the present paper the hybrid peptides of P6A and RGD, namely ARPAKRGDS 17, ARPAKRGDV19, ARPAKRGDF 21, QRPAKRGDS 18, QRPAKRGDV 20 and QRPAKRGDF 22, were synthesized via the solution method, segment condensation and TFA/TFMS A-catalyzed deprotection (in