N-α-Benzoyl-DL-arginine-p-nitroanilide hydrochloride
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N-α-Benzoyl-DL-arginine-p-nitroanilide hydrochloride
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CAS No:
911-77-3
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Formula:
C19H22N6O4.ClH
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Chemical Name:
N-α-Benzoyl-DL-arginine-p-nitroanilide hydrochloride
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Synonyms:
Benzamide,N-[4-[(aminoiminomethyl)amino]-1-[[(4-nitrophenyl)amino]carbonyl]butyl]-,hydrochloride (1:1);Valeranilide,2-benzamido-5-guanidino-4′-nitro-,monohydrochloride,DL-;Benzamide,N-[4-[(aminoiminomethyl)amino]-1-[[(4-nitrophenyl)amino]carbonyl]butyl]-,monohydrochloride,(±)-;Benzamide,N-[4-[(aminoiminomethyl)amino]-1-[[(4-nitrophenyl)amino]carbonyl]butyl]-,monohydrochloride;Nα-Benzoyl-DL-arginine-p-nitroanilide hydrochloride;NSC 83264;N-α-Benzoyl-DL-arginine-p-nitroanilide hydrochloride;99671-52-0;37039-24-0
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CAS No:
Description
Light yellow fine crystalline powder
A chromogenic substrate that permits direct measurement of peptide hydrolase activity, e.g., papain and trypsin, by colorimetry. The substrate liberates p-nitroaniline as a chromogenic product.
N-α-Benzoyl-DL-arginine-p-nitroanilide hydrochloride Basic Attributes
434.88
434.146942
213-011-2
29252900
Drug Information
Colorless, endogenous or exogenous pigment precursors that may be transformed by biological mechanisms into colored compounds; used in biochemical assays and in diagnosis as indicators, especially in the form of enzyme substrates. Synonym: chromogens (not to be confused with pigment-synthesizing bacteria also called chromogens). (See all compounds classified as Chromogenic Compounds.)
BAPNA
N-α-Benzoyl-DL-arginine-p-nitroanilide hydrochloride Use and Manufacturing
Substrate for trypsin, papain, ficin, bromelain, plasmin, and cathepsin B.
Computed Properties
Molecular Weight:434.9
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:434.1469309
Monoisotopic Mass:434.1469309
Topological Polar Surface Area:168
Heavy Atom Count:30
Complexity:588
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Recommended Suppliers of N-α-Benzoyl-DL-arginine-p-nitroanilide hydrochloride
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N-α-Benzoyl-DL-arginine-p-nitroanilide hydrochloride
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