NAlpha-Boc-L-histidine

CAS: 17791-52-5

Ref. TR-B656225

Produktinformation

• Name: NAlpha-Boc-L-histidine
• Synonyme: N-[(1,1-Dimethylethoxy)carbonyl]-L-histidine, N-Carboxy-L-histidine N-tert-Butyl Ester, (tert-Butoxycarbonyl)-L-histidine, (tert-Butoxycarbonyl)histidine, N-(tert-Butoxycarbonyl)histidine, N-tert-Butoxycarbonyl-L-histidine, N-tert-Butyloxycarbonyl-L-histidine, NSC 334942, tert-Butyloxycarbonyl-L-histidine, (+)-Na-(tert-Butoxycarbonyl)-L-histidine, Na-(tert-Butyloxycarbonyl)-L-histidine, Na-tert-Butoxycarbonyl-L-histidine, (+)-N^α-(tert-Butoxycarbonyl)-<span class="text-smallcaps">L</span>-histidine, (2S)-2-[(tert-butoxycarbonyl)amino]-3-(1H-imidazol-5-yl)propanoate, (2S)-2-[[(tert-Butoxy)carbonyl]amino]-3-(1H-imidazol-4-yl)propanoic acid, (2S)-3-(1H-Imidazol-3-ium-5-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate, (tert-Butoxycarbonyl)-<span class="text-smallcaps">L</span>-histidine, <span class="text-smallcaps">L</span>-Histidine, N-[(1,1-dimethylethoxy)carbonyl]-, Boc-His-OH, Histidine, N-carboxy-, N-tert-butyl ester, Histidine, N-carboxy-, N-tert-butyl ester, <span class="text-smallcaps">L</span>-, N(alpha)-boc-l-histidine, N-(tert-butoxycarbonyl)-L-histidine, N-(tert-butoxycarbonyl)histidine, N-Boc-L-Histidine, N-[(1,1-Dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-histidine, N-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-histidine, N-tert-Butyloxycarbonyl-<span class="text-smallcaps">L</span>-histidine, N-α-Boc-L-histidine, N^α-(tert-Butyloxycarbonyl)-<span class="text-smallcaps">L</span>-histidine, tert-Butyloxycarbonyl-<span class="text-smallcaps">L</span>-histidine, Histidine, N-carboxy-, N-tert-butyl ester, L-, L-Histidine, N-[(1,1-dimethylethoxy)carbonyl]-

Beschreibung

Applications Nα-Boc-L-histidine is an N-Boc-protected form of L-Histidine (H456010). L-Histidine is an essential amino acid that plays an important role in mitochondrial glutamine transport and has potential of abolishing oxidative stress caused by brain edema.L-Histidine promotes zinc uptake in human erythrocyes and also has potential as an antioxidant therapy for acute mammary inflammation in cattle.
References Chaiyotwittayakun, A., et al.: J. Dairy Sci., 85, 60 (2002); Horn, N., et al.: J. Phys., 489, 73 (1995); Rama Rao, K., et al.: Am. J. Path., 176, 1400 (2010);

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 255.27
• Formel: C₁₁H₁₇N₃O₄
• Farbe/Form: Neat
• InChl: InChI=1S/C11H17N3O4/c1-11(2,3)18-10(17)14-8(9(15)16)4-7-5-12-6-13-7/h5-6,8H,4H2,1-3H3,(H,12,13)(H,14,17)(H,15,16)/t8-/m0/s1
• InChI Key: InChIKey=QGZKDVFQNNGYKY-UHFFFAOYSA-N
• SMILES: COc1cc(I)c(CC#N)cc1OC