| Identification | Back Directory | [Name]
N-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE | [CAS]
2440-62-2 | [Synonyms]
Suphepa
SUC-F-PNA
SUC-PHE-PNA
(S)-4-((2-((4-Nitrop
SUC-PHENYLALANINE-PNA
substrateforchymotrypsin
N-(Suc-L-Phe-)-4-Nitroaniline
SUCCINYL-L-PHENYLALANINE 4-NITROANILIDE
N-SUCCINYL-L-PHENYALANINE-P-NITROANILIDE
N-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE
L-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE
N-(4-Nitrophenyl)-Nα-Suc-L-phenylalaninamide
N-succinyl-L-phenylalanine-P-*nitroanilide crysta
N-SUCCINYL-L-PHENYLALANINE-P-*NITROANILI DE CRYSTALL
n-Succinyl-L-phenylalanine-p-nitroanilidecrystalline
Na-(3-Carboxypropionyl)-1-phenylalanine-4-nitroanilide
N-(4-Nitrophenyl)-Nα-(3-carboxypropionyl)phenylalaninamide
Nα-(3-Carboxypropionyl)-N-(4-nitrophenyl)phenylalaninamide
N-Succinyl-L-phenylalanine-p-nitroanilide protease substrate
N-(4-Nitrophenyl)-Nα-(3-carboxypropanoyl)-L-phenylalaninamide
4-[[1-(benzyl)-2-keto-2-(4-nitroanilino)ethyl]amino]-4-keto-butyric acid
4-[[1-(4-nitroanilino)-1-oxo-3-phenylpropan-2-yl]amino]-4-oxobutanoic acid
4-({1-benzyl-2-[(4-nitrophenyl)amino]-2-oxoethyl}amino)-4-oxobutanoic acid
4-[[1-(benzyl)-2-keto-2-[(4-nitrophenyl)amino]ethyl]amino]-4-keto-butyric acid
4-[[2-[(4-nitrophenyl)amino]-2-oxo-1-(phenylmethyl)ethyl]amino]-4-oxobutanoic acid
4-[[1-[(4-nitrophenyl)amino]-1-oxo-3-phenyl-propan-2-yl]amino]-4-oxo-butanoic acid
4-[[2-[(4-nitrophenyl)amino]-2-oxo-1-(phenylmethyl)ethyl]amino]-4-oxo-butanoic acid
(S)-4-[[2-[(4-nitrophenyl)amino]-2-oxo-1-(phenylmethyl)ethyl]amino]-4-oxobutyric acid
4-[[(S)-2-[(4-Nitrophenyl)amino]-2-oxo-1-(phenylmethyl)ethyl]amino]-4-oxobutanoic acid
Butanoic acid, 4-[[(1S)-2-[(4-nitrophenyl)amino]-2-oxo-1-(phenylmethyl)ethyl]amino]-4-oxo- | [EINECS(EC#)]
219-472-6 | [Molecular Formula]
C19H19N3O6 | [MDL Number]
MFCD00047721 | [MOL File]
2440-62-2.mol | [Molecular Weight]
385.37 |
| Hazard Information | Back Directory | [Uses]
N-Succinyl-L-phenylalanine-p-nitroanilide has been used as a substrate for the hydrolytic activity of chymotrypsin and molar absorptive experiments. It has also been used for monitoring in vitro α-chymotrypsin inhibition assay. | [Biochem/physiol Actions]
N-Succinyl-L-phenylalanine-p-nitroanilide, a substrate for the hydrolytic activity of chymotrypsin, forms a yellow chromophore, p-nitroaniline, which can be measured spectrophotometrically at 410 nm. |
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