ChemicalBook--->CAS DataBase List--->76626-41-0

76626-41-0

76626-41-0 Structure

76626-41-0 Structure
IdentificationBack Directory
[Name]

D-ILE-PHE-LYS P-NITROANILIDE
[CAS]

76626-41-0
[Synonyms]

IFK-PNA
H-D-Ile-FK-pNA
H-D-ILE-PHE-LYS-PNA
D-ILE-PHE-LYS P-NITROANILIDE
D-ILE-PHE-LYS P-(D-ILE-PHE-LYS P-NITROANILIDE)
D-isoleucine-phenylalanine-lysine-p-nitroanilide
D-Isoleucyl-L-phenylalanyl-N-(4-nitrophenyl)-L-lysinamide
L-Lysinamide, D-isoleucyl-L-phenylalanyl-N-(4-nitrophenyl)-
(2S)-6-amino-2-[[(2S)-2-[[(2R,3R)-2-amino-3-methylpentanoyl]amino]-3-phenylpropanoyl]amino]-N-(4-nitrophenyl)hexanamide
[Molecular Formula]

C27H38N6O5
[MDL Number]

MFCD00038844
[MOL File]

76626-41-0.mol
[Molecular Weight]

526.63
Chemical PropertiesBack Directory
[Boiling point ]

851.5±65.0 °C(Predicted)
[density ]

1.223±0.06 g/cm3(Predicted)
[storage temp. ]

−20°C
[pka]

12.43±0.70(Predicted)
[Sequence]

{d-Ile}-Phe-{Lys-pNA}
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

D-Ile-Phe-Lys-pNA is a highly specific substrate for human plasmin[1][2].
[References]

[1] G C Szabó, et al. Specificity of pancreatic elastase with tripeptidyl-p-nitroanilide substrates. Acta Biochim Biophys Acad Sci Hung. 1980;15(4):263-763. PMID:6945027
[2] M Pozsgay, et al. Study of the specificity of thrombin with tripeptidyl-p-nitroanilide substrates. Eur J Biochem. 1981 Apr;115(3):491-5. DOI:10.1111/j.1432-1033.1981.tb06229.x
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