CAS 87764-47-4
:4-Deoxy-4-Fluoro-D-Mannose
Description:
4-Deoxy-4-Fluoro-D-Mannose is a fluorinated monosaccharide derivative of mannose, characterized by the substitution of a fluorine atom at the 4-position of the sugar molecule. This modification can significantly influence its biochemical properties and interactions. The compound typically exists as a white to off-white solid and is soluble in polar solvents such as water and methanol, which is common for many sugars and their derivatives. Its molecular structure includes a six-membered pyranose ring, which is a common feature in carbohydrate chemistry. The presence of the fluorine atom can enhance the compound's stability and alter its reactivity, making it of interest in various fields, including medicinal chemistry and biochemistry. 4-Deoxy-4-Fluoro-D-Mannose may also exhibit unique biological activities, potentially serving as a tool for studying carbohydrate-protein interactions or as a precursor in the synthesis of more complex molecules. As with any chemical substance, proper handling and safety precautions should be observed due to potential reactivity and biological effects.
Formula:C6H11FO5
InChI:InChI=1/C6H11FO5/c7-5(3(10)1-8)6(12)4(11)2-9/h2-6,8,10-12H,1H2/t3-,4-,5-,6-/m1/s1
SMILES:C([C@H]([C@H]([C@@H]([C@@H](C=O)O)O)F)O)O
Synonyms:- 4-Deoxy-4-fluoromannose
- D-Mannose, 4-deoxy-4-fluoro-
- 4-Deoxy-4-fluoro-D-mannose
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Found 5 products.
4-Deoxy-4-fluoro-D-mannose
CAS:<p>4-Deoxy-4-fluoro-D-mannose is a sugar that is an analog of 3-deoxy-3-fluoro-d-mannose. It is synthesized by the transfer of a 6-hydroxyl group from 6,6'-dideoxyadenosine to the C6 hydroxyl group of 3,6'-dihexadecylthio adenosine. 4,4'-Difluoro D-mannose is then obtained by hydrolysis and decarboxylation. This process can be catalyzed by enzyme catalysis with phosphofructokinase or hexokinase. 4,4'-Difluoro D mannose has been used in biochemical studies as an analog for 6,6'-dideoxydaunosine. It has also been used as a substrate for virus glycosylation and protein glycosylation in living cells. In addition, it has been shown to inhibit</p>Formula:C6H11FO5Purity:Min. 95%Color and Shape:PowderMolecular weight:182.15 g/mol4-Deoxy-4-fluoro-D-mannose
CAS:Controlled Product<p>Applications Shown to be metabolized in yeast. Also shown to interfere with the glycosylation of viral G-protein in vesicular-stomatitis-virus-infected BHK cells.<br>References Biochem. J., 209 (3), 677-685 (1983), J. Biol. Chem., 259, 1027-1030 (1984)<br></p>Formula:C6H11FO5Color and Shape:NeatMolecular weight:182.15




