CAS 34213-86-0

p-Aminophenyl α-D-mannopyranoside

Description:

p-Aminophenyl α-D-mannopyranoside is a chemical compound characterized by its structure, which consists of a p-aminophenyl group linked to an α-D-mannopyranoside moiety. This compound is a glycoside, meaning it contains a sugar component (in this case, mannose) bonded to a non-sugar moiety (the p-aminophenyl group). It is typically a white to off-white solid and is soluble in water due to the presence of the sugar unit, which enhances its hydrophilicity. The p-aminophenyl group can participate in various chemical reactions, making this compound useful in biochemical applications, including as a substrate in enzyme assays or as a building block in the synthesis of more complex molecules. Additionally, the presence of the amino group can facilitate further functionalization, allowing for the development of derivatives with tailored properties. Its CAS number, 34213-86-0, is a unique identifier that can be used to find more detailed information about its properties, safety data, and applications in scientific literature.

Formula: C₁₂H₁₇NO₆

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: O([C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O)C2=CC=C(N)C=C2

Synonyms:

• 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
• (2R,3S,4S,5S,6R)
• p-aminophenyl alpha-D-mannoside
• (2R,3S,4S,5S,6R)-2-(4-Aminophenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
• (2R,3S,4S,5S,6R)-2-(4-aminophenoxy)-6-methylol-tetrahydropyran-3,4,5-triol
• -2-(4-Aminophenoxy)
• (2R,3S,4S,5S,6R)-2-(4-aminophenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol
• P-AMINOPHENYL-A-D-MANNOPYRANOSIDECRYSTAL LINE
• (2R,3S,4S,5S,6R)-2-(4-azanylphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol
• 4-Aminophenyl α-D-mannopyranoside ,98%

P-AMINOPHENYL α-D-MANNOPYRANOSIDE

CAS: 34213-86-0

Formula: C₁₂H₁₇NO₆

Purity: 98%

Color and Shape: Solid

Molecular weight: 271.2665

Ref: IN-DA00C0PJ

4-Aminophenyl α-D-mannopyranoside

CAS: 34213-86-0

Formula: C₁₂H₁₇NO₆

Purity: ≥ 98%

Color and Shape: White to off-white crystalline powder

Molecular weight: 271.27

Ref: 7W-GC3242

4-Aminophenyl α-D-mannopyranoside

CAS: 34213-86-0

4-Aminophenyl α-D-mannopyranoside

Purity: 98%

Molecular weight: 271.27g/mol

Ref: 54-BICL4240

4-Aminophenyl a-D-mannopyranoside

CAS: 34213-86-0

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.

Formula: C₁₂H₁₇NO₆

Purity: Min. 95%

Color and Shape: Off-White Powder

Molecular weight: 271.27 g/mol

Ref: 3D-MA04337

4-Aminophenyl α-D-Mannopyranoside

Controlled Product

CAS: 34213-86-0

Stability Hygroscopic
Applications Increases the uptake rate of liposomes.
References Chono, S., et al.: J. Pharm., Pharmacol., 59, 75 (2007), VeeraReddy, P., et al.: J. Drug Target., 17, 140 (2009),

Formula: C₁₂H₁₇NO₆

Color and Shape: Neat

Molecular weight: 271.27

Ref: TR-A624995