Z-L-tyrosine amide

CAS : 19898-39-6

Ref. 3D-FT47844

Informations sur le produit

• Nom: Z-L-tyrosine amide
• Synonymes: Z-L-Tyr-NH2, Carbamic acid, (α-carbamoyl-p-hydroxyphenethyl)-, benzyl ester, <span class="text-smallcaps">L</span>-, Carbamic acid, N-[(1S)-2-amino-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-, phenylmethyl ester, Carbamic acid, [(2S)-2-amino-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-, phenylmethyl ester, Carbamic acid, [2-amino-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-, phenylmethyl ester, (S)-, N-(Benzyloxycarbonyl)-<span class="text-smallcaps">L</span>-tyrosinamide, N-Carbobenzoxy-<span class="text-smallcaps">L</span>-tyrosinamide, NSC 333738, Nalpha-[(benzyloxy)carbonyl]tyrosinamide, Phenylmethyl N-[(1S)-2-amino-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]carbamate

Description

Z-L-tyrosine amide is a synthetic amino acid with the chemical formula HOOCCH(NH)CH(COOC)CH(NH)COOH. It is the amide of L-tyrosine and pyruvic acid. The compound has been shown to be an inhibitor of histidine decarboxylase and an antagonist of glutamate receptors. Z-L-tyrosine amide also exhibits some anti-inflammatory properties, which may result from its ability to inhibit prostaglandin synthesis. The structure of this molecule consists of a hydrocinnamic acid group, a reactive chloromethyl ketone residue, and a pyrrolidone ring that is activated by the carboxylate group. The active site of this molecule is inactivated by the presence of the chloromethyl ketone residue. Z-L-tyrosine amide is prepared in two steps from L-histidine methyl ester hydrochloride

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 314.34 g/mol
• Formule: C₁₇H₁₈N₂O₄
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C17H18N2O4/c18-16(21)15(10-12-6-8-14(20)9-7-12)19-17(22)23-11-13-4-2-1-3-5-13/h1-9,15,20H,10-11H2,(H2,18,21)(H,19,22)/t15-/m0/s1
• Code InChI: InChIKey=DJPCVJYIWLEUBO-HNNXBMFYSA-N
• SMILES: NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)OCc1ccccc1