N-alpha-Benzoyl-L-histidine

CAS: 5354-94-9

Ref. 3D-FB47552

Produktinformation

• Name: N-alpha-Benzoyl-L-histidine
• Synonyme: Bz-L-His-OH, (2S)-2-Benzamido-3-(1H-imidazol-3-ium-5-yl)propanoate, (2S)-3-(1H-Imidazol-4-yl)-2-(phenylformamido)propanoic acid, (S)-2-Benzoylamino-3-(1H-imidazol-4-yl)propanoic acid, <span class="text-smallcaps">L</span>-Histidine, N-benzoyl-, Histidine, N-benzoyl-, <span class="text-smallcaps">L</span>-, N-Alpha-Benzoyl-L-Histidine, N-Benzoyl-<span class="text-smallcaps">L</span>-histidine, N-Benzoylhistidine, N^α-Benzoyl-<span class="text-smallcaps">L</span>-histidine, N^α-Benzoylhistidine, NSC 306118, α-N-Benzoyl-<span class="text-smallcaps">L</span>-histidine
• CAS: 5354-94-9

Beschreibung

Benzoyl-L-histidine is a derivative of the amino acid histidine, which is a regulatory molecule in biochemical reactions. It has been shown to be an isomeric form of benzoyl-L-histidine. Benzoyl-L-histidine has been shown to be oxidized by bromoacetic acid and titrated with potassium permanganate. This reaction produces a residue, which can be quantified by the use of a thiolate reagent and model system. Benzoyl-L-histidine has two isomers: monosubstituted and disubstituted. The kinetic properties of this compound have also been studied in a model protein system.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 259.26 g/mol
• Formel: C₁₃H₁₃N₃O₃
• Reinheit: Min. 95%
• InChl: InChI=1S/C13H13N3O3/c17-12(9-4-2-1-3-5-9)16-11(13(18)19)6-10-7-14-8-15-10/h1-5,7-8,11H,6H2,(H,14,15)(H,16,17)(H,18,19)/t11-/m0/s1
• InChI Key: InChIKey=AUDPUFBIVWMAED-NSHDSACASA-N
• SMILES: O=C(N[C@@H](Cc1cnc[nH]1)C(=O)O)c1ccccc1