Benzoyl-L-arginine p-nitroanilide monohydrochloride

Product Description

Benzoyl-L-arginine p-nitroanilide monohydrochloride
Catalog number: MDP0078
CAS Number: 134720-03-9
Sequence: Benzoyl-L-arginine p-nitroanilide monohydrochloride
Amount: 100 mg
Molecular Weight: 398.4 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.

References:
1: 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.
2: Butterworth J, Duncan JJ. The hydrolysis of N-benzoyl-L-phenylalanyl-L-valyl-L-arginine-p-nitroanilide and its use as a substrate for the assay of cathepsin B Anal Biochem. 1980 Jul 15;106(1):156-62.
3: 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.
4: Dietz AA, Rubinstein HM, Hodges LK. Use of alpha-N-benzoyl-L-arginine-p-nitroanilide as trypsin substrate in estimation of alpha 1-antitrypsin Clin Chem. 1976 Oct;22(10):1754-5.
5: Tokura S, Nishi N, Noguchi J. A new substrate for papain, benzoyl-L-arginine-p-nitroanilide (L-BAPA) J Biochem. 1971 Mar;69(3):599-600.
6: Mole JE, Horton HR. Kinetics of papain-catalyzed hydrolysis of -N-benzoyl-L-arginine-p-nitroanilide Biochemistry. 1973 Feb 27;12(5):816-22.
7: Gofshtein-Gandman LV, Keynan A, Milner Y. Bacteria of the genus Bacillus have a hydrolase stereospecific to the D isomer of benzoyl-arginine-p-nitroanilide J Bacteriol. 1988 Dec;170(12):5895-900.
8: Sousa MO, Rodrigues CV, Pena HB, Alvarenga MG, Machado-Coelho GL, Santoro MM, Juliano MA, Juliano L, Figueiredo AF. Kinetic characterization of rat tissue kallikrein using N alpha-substituted arginine 4-nitroanilides and N alpha-benzoyl-L-arginine ethyl ester as substrates Braz J Med Biol Res. 1996 Mar;29(3):327-34.
9: Nakata H, Ishii SI. Substrate activation in the trypsin-catalyzed hydrolysis of benzoyl-L-arginine p-nitroanilide Biochem Biophys Res Commun. 1970 Oct 23;41(2):393-400.
10: Malis F, Kasafírek E, Fric P, Josífko M. Use of a new synthetic substrate, Nalpha-tosyl-L-arginine-P-nitroanilide (TAPA), for determining trypsin activity in the duodenal contents Acta Univ Carol Med Monogr. 1977;(79 Pt 3):131-8.

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