N6-Carbobenzyloxy-L-lysine benzyl ester hydrochloride

CAS: 6366-70-7

Ref. 3D-FC19710

Product Information

• Name: N6-Carbobenzyloxy-L-lysine benzyl ester hydrochloride
• Synonyms: N6-[(Phenylmethoxy)carbonyl]-L-lysine phenylmethyl ester hydrochlorideN6-Carbobenzoxy-L-lysine benzyl ester hydrochlorideNSC 88180, (2S)-1-(benzyloxy)-1-oxo-6-{[(phenylacetyl)oxy]amino}hexan-2-aminium chloride, (S)-Benzyl 2-amino-6-(((benzyloxy)carbonyl)amino)hexanoate hydrochloride, <span class="text-smallcaps">L</span>-Lysine, N⁶-[(phenylmethoxy)carbonyl]-, phenylmethyl ester, hydrochloride (1:1), <span class="text-smallcaps">L</span>-Lysine, N⁶-[(phenylmethoxy)carbonyl]-, phenylmethyl ester, monohydrochloride, H-Lys(Cbz)-OBzl.HCl, H-Lys(Z)-OBzl.HCl, Lysine, N⁶-carboxy-, dibenzyl ester, hydrochloride, Lysine, N⁶-carboxy-, dibenzyl ester, hydrochloride, <span class="text-smallcaps">L</span>-, N-e-CBZ-L-Lys-OBzl HCl, N-epsilon-benzyloxycarbonyl-l-lysine benzyl ester hydrochloride, N-epsilon-cbz-L-lysine benzyl ester*hydrochloride, N6-Cbz-L-Lysine benzyl ester hydrochloride, N⁶-Carbobenzoxy-<span class="text-smallcaps">L</span>-lysine benzyl ester hydrochloride, NSC 88180, Nepsilon-Benzyloxycarbonyl-L-Lysine Benzyl Ester Hydrochloride, benzyl N6-[(benzyloxy)carbonyl]lysinate, benzyl N6-benzyloxycarbonyl-L-lysinate hydrochloride, L-Lysine, N6-[(phenylmethoxy)carbonyl]-, phenylmethyl ester, hydrochloride (1:1), N6-Carbobenzoxy-L-lysine benzyl ester hydrochloride, L-Lysine, N6-[(phenylmethoxy)carbonyl]-, phenylmethyl ester, monohydrochloride, Lysine, N6-carboxy-, dibenzyl ester, hydrochloride, L-, Lysine, N6-carboxy-, dibenzyl ester, hydrochloride

Description

N6-Carbobenzyloxy-L-lysine benzyl ester hydrochloride is a chiral compound with an asymmetric carbon atom. It is an inhibitor of the enzyme aspartate transaminase, which converts amino acids into ammonia and alpha keto acid. This inhibition leads to an overload of ammonia in the body and thus to cardiac, colitis, bronchial, and myosis disorders. N6-Carbobenzyloxy-L-lysine benzyl ester hydrochloride binds to the active site of aspartate transaminase and blocks its activity. The phenyl group attached to nitrogen atom forms a covalent bond with the active site of aspartate transaminase, thereby inhibiting its activity.

• Brand: Biosynth

Chemical properties

• Molecular weight: 406.9 g/mol
• Formula: C₂₁H₂₇ClN₂O₄
• Purity: Min. 95%