Z-glu(OBzl)-OH NA

CAS : 5680-86-4

Ref. 3D-FG38037

Informations sur le produit

• Nom: Z-glu(OBzl)-OH NA
• Synonymes: (2S)-5-(benzyloxy)-2-{[(benzyloxy)carbonyl]amino}-5-oxopentanoic acid (non-preferred name), (2S)-5-Oxo-5-phenylmethoxy-2-(phenylmethoxycarbonylamino)pentanoic acid, (S)-2-Benzyloxycarbonylamino-pentanedioic acid 5-benzyl ester, 5-(Benzyloxy)-2-{[(Benzyloxy)Carbonyl]Amino}-5-Oxopentanoic Acid (Non-Preferred Name), 5-(Phenylmethyl) hydrogen N-[(phenylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-glutamate, <span class="text-smallcaps">L</span>-Glutamic acid, N-[(phenylmethoxy)carbonyl]-, 5-(phenylmethyl) ester, Carbobenzoxy-<span class="text-smallcaps">L</span>-glutamic acid γ-benzyl ester, Cbz-Glu(OBzl)-OH, Cbz-L-Glutamic Acid-r-Benyzl Ester, Cbz-L-glutamic acid 5-benzyl ester, Glutamic acid, N-carboxy-, N,5-dibenzyl ester, <span class="text-smallcaps">L</span>-, N-(Benzyloxycarbonyl)-<span class="text-smallcaps">L</span>-glutamic acid γ-benzyl ester, N-CBZ-L-Glutamic Acid Gamma-Benzyl Ester, N-Carbobenzoxy-<span class="text-smallcaps">L</span>-glutamic acid 5-benzyl ester, N-Carbobenzoxy-<span class="text-smallcaps">L</span>-glutamic acid γ-benzyl ester, N-Carbobenzyloxy-<span class="text-smallcaps">L</span>-glutamic acid γ-benzyl ester, N-a-CBZ-(g-OBzl)-D-Glu, NSC 169178, Z-Glutamic Acid-O Benzyl Ester, γ-Benzyl N-(benzyloxycarbonyl)-<span class="text-smallcaps">L</span>-glutamate, L-Glutamic acid, N-[(phenylmethoxy)carbonyl]-, 5-(phenylmethyl) ester, Glutamic acid, N-carboxy-, N,5-dibenzyl ester, L-, γ-Benzyl N-(benzyloxycarbonyl)-L-glutamate, 5-(Phenylmethyl) hydrogen N-[(phenylmethoxy)carbonyl]-L-glutamate, N-Carbobenzoxy-L-glutamic acid 5-benzyl ester

Description

NA is a hydrophobic molecule that has been synthesised to be prebiotic. It has been shown to have high specificity for the amination reaction, which is a synthetic reaction. NA can also be synthesised from sequences of pre-existing polypeptides, and homochiral NA can be obtained by using the rotator technique. The reaction time for the synthesis of NA is short, and it can be activated with l-glutamic acid or norvaline. The biological properties of NA are still being studied, but it has been shown to have anti-inflammatory activities in vitro.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 371.38 g/mol
• Formule: C₂₀H₂₁NO₆
• Degré de pureté: Min. 95%