N-Acetyl-L-glutamic-2,3,3,4,4-d5 Acid

CAS : 1188-37-0

Ref. TR-A178256

Informations sur le produit

• Nom: N-Acetyl-L-glutamic-2,3,3,4,4-d5 Acid
• Synonymes: (2S)-2-Acetamidopentanedioic-2,3,3,4,4-d5 acid, (2S)-2-(acetylamino)pentanedioate, (2S)-2-Acetamidopentanedioic acid, <span class="text-smallcaps">L</span>-Glutamic acid, N-acetyl-, <span class="text-smallcaps">L</span>-N-Acetylglutamic acid, Ac-Glu-OH, Ac-Gly, Acetyl-L-glutamic acid, Acetylglutamic acid, Glutamic acid, N-acetyl-, <span class="text-smallcaps">L</span>-, N-Acetyl-<span class="text-smallcaps">L</span>-glutamic acid, N-Acetyl-<span class="text-smallcaps">L</span>-glutaminic acid, N-Acetyl-L-glutamate, N-Acetyl-L-glutamic acid, N-Acetyl-S-glutamic acid, N-Acetylglutamate, N-acetylglutamic acid, α-(N-Acetyl)-<span class="text-smallcaps">L</span>-glutamic acid, Glutamic acid, N-acetyl-, L-, L-Glutamic acid, N-acetyl-

Description

Applications N-Acetyl-L-glutamic-2,3,3,4,4-d5 Acid is the deuterium labelled form of N-Acetyl-L-glutamic Acid (A178255), which is the N-Acetyl analogue of the non-essential amino acid L-glutamic acid (G596960). N-Acetyl-L-glutamic Acid activates carbamoyl phosphate synthetase in the urea cycle.
References Saheki, T. et al.: J. Biochem., 77, 659 (1975); Rivas, J. et al.: Acta Biol. Med. Ger., 36, 1673 (1977); Zollner, H.: Biochim. Biophys. Acta, 676, 170 (1981);

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 194.2
• Formule: C₇D₅H₆NO₅
• Couleur/Forme: Neat
• InChI: InChI=1S/C7H11NO5/c1-4(9)8-5(7(12)13)2-3-6(10)11/h5H,2-3H2,1H3,(H,8,9)(H,10,11)(H,12,13)/t5-/m0/s1/i2D2,3D2,5D
• Code InChI: InChIKey=RFMMMVDNIPUKGG-ARCCNJGNSA-N
• SMILES: [2H]C([2H])(C(=O)O)C([2H])([2H])[C@]([2H])(NC(C)=O)C(=O)O