N-α-Benzoyl-L-arginine amide hydrochloride

CAS: 4299-03-0

Ref. 3D-FB49071

Product Information

• Name: N-α-Benzoyl-L-arginine amide hydrochloride
• Synonyms: Bz-L-Arg-NH2·HCl, Benzamide, N-(1-carbamoyl-4-guanidinobutyl)-, monohydrochloride, <span class="text-smallcaps">L</span>-, Benzamide, N-[1-(aminocarbonyl)-4-[(aminoiminomethyl)amino]butyl]-, monohydrochloride, (S)-, Benzoyl-<span class="text-smallcaps">L</span>-arginine amide monohydrochloride, Benzoyl-Arg-NH2.HCl, Bz-Arg-NH2 . HCl, N-carbamoyl-4-{4-[(diaminomethylidene)amino]butyl}benzamide hydrochloride (1:1), N-{1-amino-5-[(diaminomethylidene)amino]-1-oxopentan-2-yl}benzamide, N-α-Benzoyl-<span class="text-smallcaps">L</span>-argininamide hydrochloride, N2-(phenylcarbonyl)-L-argininamide hydrochloride, NSC 343719, α-N-Benzoyl-<span class="text-smallcaps">L</span>-argininamide hydrochloride, Benzoyl-L-arginine amide monohydrochloride, α-N-Benzoyl-L-argininamide hydrochloride, Benzamide, N-(1-carbamoyl-4-guanidinobutyl)-, monohydrochloride, L-

Description

N-alpha-Benzoyl-L-arginine amide hydrochloride (BA) is a synthetic, noncompetitive inhibitor of phosphodiesterase. It has been shown to inhibit protease activity in vitro and rhizosphere enzyme activities in vivo. BA also inhibits the formation of hippuric acid from benzoic acid, which is a reaction catalyzed by the enzyme phosphatase. The kinetics of this inhibition have been studied using a number of different substrates and enzymes. BA binds to the catalytic site on the enzyme, sterically hindering binding of the substrate and preventing hydrolysis.

• Brand: Biosynth

Chemical properties

• Molecular weight: 313.78 g/mol
• Formula: C₁₃H₁₉N₅O₂·HCl
• Purity: Min. 95%
• Color/Form: Powder