H-PRO-THR-GLU-PHE-P-NITRO-PHE-ARG-LEU-OH
H-PRO-THR-GLU-PHE-P-NITRO-PHE-ARG-LEU-OH Basic information
- Product Name:
- H-PRO-THR-GLU-PHE-P-NITRO-PHE-ARG-LEU-OH
- Synonyms:
-
- H-PRO-THR-GLU-PHE-PHE(4-NO2)-ARG-LEU-OH
- H-PRO-THR-GLU-PHE-P-NITRO-PHE-ARG-LEU-OH
- prolyl-threonyl-glutamyl-phenylalanyl-4-nitrophenylalanyl-arginyl-leucine
- L-Leucine, L-prolyl-L-threonyl-L-α-glutamyl-L-phenylalanyl-4-nitro-L-phenylalanyl-L-arginyl-
- PTEF-{p-nitro-Phe}-RL
- CAS:
- 90331-82-1
- MF:
- C44H63N11O13
- MW:
- 954.04
- Mol File:
- 90331-82-1.mol
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H-PRO-THR-GLU-PHE-P-NITRO-PHE-ARG-LEU-OH Chemical Properties
- Density
- 1.45±0.1 g/cm3(Predicted)
- pka
- 3.38±0.10(Predicted)
- Sequence
- Pro-Thr-Glu-Phe-{p-nitro-Phe}-Arg-Leu
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H-PRO-THR-GLU-PHE-P-NITRO-PHE-ARG-LEU-OH Usage And Synthesis
Uses
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].
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. DOI:10.1128/AAC.39.2.374
[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. DOI:10.1515/BC.2005.080
H-PRO-THR-GLU-PHE-P-NITRO-PHE-ARG-LEU-OHSupplier
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