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

Modify Date: 2025-08-23 12:26:12

H-Pro-Thr-Glu-Phe-p-nitro-Phe-Arg-Leu-OH Structure
H-Pro-Thr-Glu-Phe-p-nitro-Phe-Arg-Leu-OH structure
 Common Name H-Pro-Thr-Glu-Phe-p-nitro-Phe-Arg-Leu-OH
CAS Number 90331-82-1 Molecular Weight 954.04
Density 1.45g/cm3 Boiling Point N/A
Molecular Formula C44H63N11O13 Melting Point N/A
MSDS N/A Flash Point N/A

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


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].

 Names

Name h-pro-thr-glu-phe-p-nitro-phe-arg-leu-oh

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

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].
Related Catalog
References

[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.  

[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.  

 Chemical & Physical Properties

Density 1.45g/cm3
Molecular Formula C44H63N11O13
Molecular Weight 954.04
Exact Mass 953.46100
PSA 389.18000
LogP 3.06870
Index of Refraction 1.653
InChIKey OHIZVORKJVKXKL-RLEGQPMYSA-N
SMILES CC(C)CC(NC(=O)C(CCCN=C(N)N)NC(=O)C(Cc1ccc([N+](=O)[O-])cc1)NC(=O)C(Cc1ccccc1)NC(=O)C(CCC(=O)O)NC(=O)C(NC(=O)C1CCCN1)C(C)O)C(=O)O
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