Benzyloxycarbonyl-L-alanyl-L-alanyl-L-leucine p-nitroanilide


Catalog Number: MDP0169 (20 mg)
Benzyloxycarbonyl-L-alanyl-L-alanyl-L-leucine p-nitroanilide is a high quality Benzyloxycarbonyl-L-alanyl-L-alanyl-L-leucine p-nitroanilide. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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Benzyloxycarbonyl-L-alanyl-L-alanyl-L-leucine p-nitroanilide
Catalog number: MDP0169
CAS Number: 194022-51-0
Sequence: Benzyloxycarbonyl-L-alanyl-L-alanyl-L-leucine p-nitroanilide
Amount: 20 mg
Molecular Weight: 527.2 g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20 °C
WARNING: For in vitro Research Use Only. NOT for use on humans or animals.
Grade: Biotechnology grade. All products are highly pure.

1: Filippova IYu, Lysogorskaya EN, Oksenoit ES, Rudenskaya GN, Stepanov VM. L-Pyroglutamyl-L-phenylalanyl-L-leucine-p-nitroanilide–a chromogenic substrate for thiol proteinase assay Anal Biochem. 1984 Dec;143(2):293-7.
2: Sharma SK, Castellino FJ. The chemical synthesis of the chromogenic substrates, H-D-Val-L-Leu-L-Lys-p-nitroanilide (S2251) and H-D-Ile-L-Pro-L-ARG-p-nitroanilide (S2288) Thromb Res. 1990 Jan 1;57(1):127-38.
3: Hayakawa T, Naruse S, Kitagawa M, Kondo T. [Elastase] Nihon Rinsho. 1995 May;53(5):1192-7.
4: Kramps JA, van Twisk C, van der Linden AC. L-Pyroglutamyl-L-prolyl-L-valine-p-nitroanilide, a highly specific substrate for granulocyte elastase Scand J Clin Lab Invest. 1983 Sep;43(5):427-32.
5: Malthouse JPG. Kinetic Studies of the Effect of pH on the Trypsin-Catalyzed Hydrolysis of N-α-benzyloxycarbonyl-l-lysine-p-nitroanilide: Mechanism of Trypsin Catalysis ACS Omega. 2020 Mar 3;5(10):4915-4923.
6: Tsunematsu H, Imamura T, Makisumi S. Kinetics of hydrolysis of Na-benzoyl-p-guanidino-L-phenylalanine p-nitroanilide by trypsin J Biochem. 1983 Jul;94(1):123-8.
7: Malthouse JPG. Correction to Kinetic Study of the Effect of pH on the Trypsin-Catalyzed Hydrolysis of N-α-benzyloxycarbonyl-l-lysine-p-nitroanilide: Mechanism of Trypsin Catalysis ACS Omega. 2020 May 26;5(22):13462.
8: Lin SH, Van Wart HE. Effect of cryosolvents and subzero temperatures on the hydrolysis of L-leucine-p-nitroanilide by porcine kidney leucine aminopeptidase Biochemistry. 1982 Oct 26;21(22):5528-33.
9: Doi M, Shioi Y, Sasa T. Purification and characterization of benzoyl-L-arginine p-nitroanilide hydrolase from etiolated leaves of Zea mays Arch Biochem Biophys. 1986 Nov 1;250(2):358-63.
10: Mackenzie NE, Malthouse JP, Scott AI. Chemical synthesis and papain-catalysed hydrolysis of N-alpha-benzyloxycarbonyl-L-lysine p-nitroanilide Biochem J. 1985 Mar 1;226(2):601-6.

Products Related to Benzyloxycarbonyl-L-alanyl-L-alanyl-L-leucine p-nitroanilide can be found at Peptides

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