L-Albizziin

CAS: 1483-07-4

Ref. TR-A512000

Produktinformation

• Name: L-Albizziin
• Synonyme: 3-[(Aminocarbonyl)amino]L-alanine, L-ß-Ureodialanine, L-2-Amino-3-ureidopropionic acid, (2R)-2-ammonio-3-(carbamoylamino)propanoate, (2S)-2-Azaniumyl-3-(carbamoylamino)propanoate, 3-(Carbamoylamino)Alanine, 3-(carbamoylamino)-L-alanine, 3-Ureido-L-alanin, 3-[(Aminocarbonyl)amino]-<span class="text-smallcaps">L</span>-alanine, <span class="text-smallcaps">L</span>-2-Amino-3-ureidopropionic acid, <span class="text-smallcaps">L</span>-Alanine, 3-[(aminocarbonyl)amino]-, <span class="text-smallcaps">L</span>-Albizziin, <span class="text-smallcaps">L</span>-Albizziine, <span class="text-smallcaps">L</span>-β-Ureidoalanine, Albizziin, Albizziin (VAN), Albizziine, Albizzin, Albizzine, L-(-)-2-Amino-3-uraeidopropionic acid, L-Ala(ureido)-OH, L-Alanine, 3-((aminocarbonyl)amino)-, L-Albizziine, L-beta-Ureidoalanine, Nsc 132089, Nsc 407273, Propionic acid, 2-amino-3-ureido-, Propionic acid, 2-amino-3-ureido-, L-
• CAS: 1483-07-4

Beschreibung

Applications: Albizziin is a glutamase inhibitor, a glutaminyl-tRNA synthetase inhibitor as well as an intermediate in the synthesis of heterocycles. It is also a potential effector group in affinity chromatography.
References Beidler, D., et al.: Biochem. Pharmacol., 58, 1067 (1999), Dassonneville, L., et al.: Biochemistry, 38, 7719 (1999), Dirsch, V., et al.: Cancer Res., 61, 5817 (2001), Merschjohann, K., et al.: Planta Med., 67, 623 (2001),

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 147.13
• Formel: C₄H₉N₃O₃
• Farbe/Form: Neat
• InChl: InChI=1S/C4H9N3O3/c5-2(3(8)9)1-7-4(6)10/h2H,1,5H2,(H,8,9)(H3,6,7,10)/t2-/m0/s1
• InChI Key: InChIKey=GZYFIMLSHBLMKF-REOHCLBHSA-N
• SMILES: NC(=O)NC[C@H](N)C(=O)O