4-Aminophenyl a-D-mannopyranoside

CAS: 34213-86-0

Rif. 3D-MA04337

Informazioni sul prodotto

• Nome: 4-Aminophenyl a-D-mannopyranoside
• Sinonimi: p-Aminophenyl a-D-mannoside, 4-Aminophenyl alpha-D-mannopyranoside, 4-Aminophenyl α-<span class="text-smallcaps">D</span>-mannopyranoside, 4-Aminophenyl α-<span class="text-smallcaps">D</span>-mannoside, 4-Aminophenyl-alpha-D-mannoside, 4-Aminophenylmannoside, Mannopyranoside, p-aminophenyl, α-<span class="text-smallcaps">D</span>-, P-Aminophenyl Alpha-D-Mannopyranoside, alpha-D-Mannopyranoside, 4-aminophenyl, p-Aminophenyl α-<span class="text-smallcaps">D</span>-mannopyranoside, α-<span class="text-smallcaps">D</span>-Mannopyranoside, 4-aminophenyl, 4-Aminophenyl α-D-mannopyranoside, α-D-Mannopyranoside, 4-aminophenyl, Mannopyranoside, p-aminophenyl, α-D-, p-Aminophenyl α-D-mannopyranoside, 4-Aminophenyl α-D-mannoside

Descrizione

4-Aminophenyl a-D-mannopyranoside is a compound that has been shown to have anti-inflammatory properties. It is also used as a starting material in the synthesis of other drugs. Rats with chronic kidney disease were given 4-aminophenyl a-D-mannopyranoside daily for three weeks, and it was found that this compound prevented the development of kidney injury markers. This drug has also been shown to be effective against mouse strains with nervous system diseases. 4-Aminophenyl a-D-mannopyranoside binds to lysine residues on proteins and prevents the interactions between these residues and the amino acid glutathione, which is required for glut1 uptake in brain cells. This uptake is essential for cellular function, and therefore 4-aminophenyl a-D-mannopyranoside may be useful as chemotherapeutic treatment for brain cancer.

• Marchio: Biosynth

Proprietà chimiche

• Peso molecolare: 271.27 g/mol
• Formula: C₁₂H₁₇NO₆
• Purezza: Min. 95%
• Colore/Forma: Off-White Powder
• InChI: InChI=1S/C12H17NO6/c13-6-1-3-7(4-2-6)18-12-11(17)10(16)9(15)8(5-14)19-12/h1-4,8-12,14-17H,5,13H2/t8-,9-,10+,11+,12+/m1/s1
• InChI key: InChIKey=MIAKOEWBCMPCQR-GCHJQGSQSA-N
• SMILES: Nc1ccc(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)cc1