Benzoyl-L-arginine amide monohydrochloride monohydrate


Catalog Number: MDP0005 (500 mg)
Benzoyl-L-arginine amide monohydrochloride monohydrate is a high quality Benzoyl-L-arginine amide monohydrochloride monohydrate. 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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Benzoyl-L-arginine amide monohydrochloride monohydrate
Catalog number: MDP0005
CAS Number: 65286-27-3
Sequence: Benzoyl-L-arginine amide monohydrochloride monohydrate
Amount: 500 mg
Molecular Weight: 277.2 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: 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.
2: Miwa N, Obata Y, Suzuki A. The effect of interaction between human urokinase and its competitive inhibitor, N alpha-benzoyl-L-arginine amide, on reduction of a specific SS bond related to enzymatic activity Biochem Biophys Res Commun. 1983 Apr 29;112(2):754-62.
3: 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.
4: Mole JE, Horton HR. Kinetics of papain-catalyzed hydrolysis of -N-benzoyl-L-arginine-p-nitroanilide Biochemistry. 1973 Feb 27;12(5):816-22.
5: Wharton CW, Cornish-Bowden A, Brocklehurst K, Crook EM. Kinetics of the hydrolysis of N-benzoyl-L-serine methyl ester catalysed by bromelain and by papain. Analysis of modifier mechanisms by lattice nomography, computational methods of parameter evaluation for substrate-activated catalyses and consequences of postulated non-productive binding in bromelain- and papain-catalysed hydrolyses Biochem J. 1974 Aug;141(2):365-381.
6: 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.
7: Lockwood TD. Biguanide is a modifiable pharmacophore for recruitment of endogenous Zn(2+) to inhibit cysteinyl cathepsins: review and implications Biometals. 2019 Aug;32(4):575-593.
8: Christensen U. pH effects in plasmin-catalysed hydrolysis of alpha-N-benzoyl-L-arginine compounds Biochim Biophys Acta. 1975 Aug 26;397(2):459-67.
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: Shimizu A, Handa K, Honda T, Abe N, Kojima T, Takahara H. Three isozymes of peptidylarginine deiminase in the chicken: molecular cloning, characterization, and tissue distribution Comp Biochem Physiol B Biochem Mol Biol. 2014 Jan;167:65-73.

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Additional information

Weight 48 oz
Dimensions 8 × 8 × 8 in

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