N-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE

N-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE Structure
CAS No.
2440-62-2
Chemical Name:
N-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE
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
CBNumber:
CB9435270
Molecular Formula:
C19H19N3O6
Molecular Weight:
385.37
MOL File:
2440-62-2.mol

N-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE Properties

Boiling point 769.3±60.0 °C(Predicted)
Density 1.383±0.06 g/cm3(Predicted)
storage temp. -20°C
pka 4.68±0.10(Predicted)

SAFETY

Risk and Safety Statements

WGK Germany  3

N-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) S2628 N-Succinyl-L-phenylalanine-p-nitroanilide protease substrate 2440-62-2 1G ₹7057.9 2022-06-14 Buy
Sigma-Aldrich(India) S2628 N-Succinyl-L-phenylalanine-p-nitroanilide protease substrate 2440-62-2 5G ₹27776.95 2022-06-14 Buy
Product number Packaging Price Buy
S2628 1G ₹7057.9 Buy
S2628 5G ₹27776.95 Buy

N-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE Chemical Properties,Uses,Production

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.

N-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE Preparation Products And Raw materials

N-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE Suppliers

Global( 48)Suppliers
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A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
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CHEMICAL LAND21 82- 2 -783 - 8063 South Korea 6315 74 Inquiry
SUCCINYL-L-PHENYLALANINE 4-NITROANILIDE SUC-PHENYLALANINE-PNA SUC-PHE-PNA N-SUCCINYL-L-PHENYALANINE-P-NITROANILIDE N-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE Na-(3-Carboxypropionyl)-1-phenylalanine-4-nitroanilide L-SUCCINYL-L-PHENYLALANINE P-NITROANILIDE N-succinyl-L-phenylalanine-P-*nitroanilide crysta (S)-4-[[2-[(4-nitrophenyl)amino]-2-oxo-1-(phenylmethyl)ethyl]amino]-4-oxobutyric acid N-SUCCINYL-L-PHENYLALANINE-P-*NITROANILI DE CRYSTALL n-Succinyl-L-phenylalanine-p-nitroanilidecrystalline substrateforchymotrypsin Suphepa 4-[[(S)-2-[(4-Nitrophenyl)amino]-2-oxo-1-(phenylmethyl)ethyl]amino]-4-oxobutanoic acid N-(4-Nitrophenyl)-Nα-(3-carboxypropanoyl)-L-phenylalaninamide N-(4-Nitrophenyl)-Nα-(3-carboxypropionyl)phenylalaninamide N-(4-Nitrophenyl)-Nα-Suc-L-phenylalaninamide N-(Suc-L-Phe-)-4-Nitroaniline Nα-(3-Carboxypropionyl)-N-(4-nitrophenyl)phenylalaninamide 4-[[1-(4-nitroanilino)-1-oxo-3-phenylpropan-2-yl]amino]-4-oxobutanoic acid 4-[[1-(benzyl)-2-keto-2-(4-nitroanilino)ethyl]amino]-4-keto-butyric acid 4-[[1-[(4-nitrophenyl)amino]-1-oxo-3-phenyl-propan-2-yl]amino]-4-oxo-butanoic acid (S)-4-((2-((4-Nitrop 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-[[2-[(4-nitrophenyl)amino]-2-oxo-1-(phenylmethyl)ethyl]amino]-4-oxo-butanoic acid SUC-F-PNA Butanoic acid, 4-[[(1S)-2-[(4-nitrophenyl)amino]-2-oxo-1-(phenylmethyl)ethyl]amino]-4-oxo- N-Succinyl-L-phenylalanine-p-nitroanilide protease substrate 2440-62-2 C19H19N3O6 BioChemical Biochemicals and Reagents Chymotrypsin, alpha Enzymes, Inhibitors, and Substrates Enzyme Substrates Substrates by Enzyme Chymotrypsin, alpha Chymotrypsin, alphaEnzyme Substrates Enzyme Substrates Protease Substrates Substrates by Enzyme