H-Pro-Thr-Glu-Phe-p-nitro-Phe-Arg-Leu-OH

H-Pro-Thr-Glu-Phe-p-nitro-Phe-Arg-Leu-OH

• CAS Number: 90331-82-1
• UNSPSC Description: H-Pro-Thr-Glu-Phe-p-nitro-Phe-Arg-Leu-OH is a water-soluble polypeptide that can serve as a substrate for cathepsin D, pepsin and pepsinogen. H-Pro-Thr-Glu-Phe-p-nitro-Phe-Arg-Leu-OH has potential applications in biochemical analysis[1][2].
• Target Antigen: Cathepsin
• Type: Peptides
• Related Pathways: Metabolic Enzyme/Protease
• Applications: Metabolism-protein/nucleotide metabolism
• Field of Research: Others
• Assay Protocol: https://www.medchemexpress.com/h-pro-thr-glu-phe-p-nitro-phe-arg-leu-oh.html
• Solubility: 10 mM in DMSO
• Smiles: [O-][N+](C(C=C1)=CC=C1C[C@@H](C(N[C@@H](CCCNC(N)=N)C(N[C@H](C(O)=O)CC(C)C)=O)=O)NC([C@@H](NC([C@H](CCC(O)=O)NC([C@H]([C@H](O)C)NC([C@@H]2CCCN2)=O)=O)=O)CC3=CC=CC=C3)=O)=O
• Molecular Weight: 954.04
• References & Citations: [2]Fuentes ME, et al. Kinetics of autocatalytic zymogen activation measured by a coupled reaction: pepsinogen autoactivation. Biol Chem. 2005 Jul;386(7):689-98.|[1]Bechtold CM, et al. Antiviral properties of aminodiol inhibitors against human immunodeficiency virus and protease. Antimicrob Agents Chemother. 1995 Feb;39(2):374-9.
• Shipping Conditions: Room temperature
• Clinical Information: No Development Reported