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  • 40010-20-6 , 4-氟代-D-半乳糖, 4-fluoro-D-galactose, FUDG, Cas:40010-20-6
  • 40010-20-6 , 4-氟代-D-半乳糖, 4-fluoro-D-galactose, FUDG, Cas:40010-20-6
40010-20-6 , 4-氟代-D-半乳糖, 4-fluoro-D-galactose, FUDG, Cas:40010-20-640010-20-6 , 4-氟代-D-半乳糖, 4-fluoro-D-galactose, FUDG, Cas:40010-20-6

40010-20-6 , 4-氟代-D-半乳糖, 4-fluoro-D-galactose, FUDG, Cas:40010-20-6

40010-20-6 , 4-氟代-D-半乳糖,
4-fluoro-D-galactose,
Cas:40010-20-6
C6H11FO5 / 182.15
MFCD00057524

4-氟代-D-半乳糖, 4-fluoro-D-galactose

4-Deoxy-4-fluoro-D-galactose (FUDG) is a modification of the sugar galactose. It is an inhibitor of glucosyltransferases, and it is used in the synthesis of oligosaccharides. FUDG has been shown to be a substrate for recombinant proteins that bind to 2-deoxy-2-fluoro-d-mannose, which are involved in the regulation of blood group expression. The binding affinity and specificity of FUDG for these proteins was examined using electrophysiology techniques. These results may help to rationalize how FUDG binds to these proteins and its potential as a glucose sensor.

4-Fluoro-4-deoxy-D-galactopyranose (4FDGal) is a monosaccharide that has gained significant attention due to its unique properties, potential applications, and interesting synthesis methods. In this paper, we will provide detailed information on the physical and chemical properties, synthesis, characterization, analytical methods, biological properties, toxicity, safety, current state of research, potential implications, limitations, and future directions of 4FDGal.

Definition and background:

4FDGal is a monosaccharide that has a fluorine atom attached to its fourth carbon atom. It is also known as 4-Fluoro-D-galactose. Galactose is a simple sugar that is a component of many carbohydrates found in food. It is particularly important in the formation of glycolipids and glycoproteins in biological processes. 4FDGal has many unique properties, such as high water solubility, and it has been used in many studies as a substitute for natural carbohydrates for its unique properties.

Synthesis and characterization:

There are various methods of synthesizing 4FDGal, including conventional methods using galactose derivatives and fluorinating agents like silver trifluoromethanesulfonate. However, the most common method is the enzymatic synthesis by using galactosyltransferases. Characterizing 4FDGal is done through many techniques including NMR spectroscopy, and Fourier-transform infrared (FTIR) spectroscopy.

Analytical methods:

The analytical methods that can be used to determine the identity and quantity of 4FDGal in a sample include high-performance liquid chromatography (HPLC), gas chromatography (GC), and mass spectrometry (MS).

Biological properties:

4FDGal has been found to have many biological properties which make it an important tool in the study of biological processes. It has been found to bind to specific lectins, which are proteins that bind to carbohydrates, with high affinity.

Toxicity and safety in scientific experiments:

Overall, 4FDGal is considered to be relatively safe and non-toxic in scientific experiments. However, as with any chemical, there are potential hazards associated with its use, and safety protocols must be followed when using it in laboratory experiments.

Applications in scientific experiments:

4FDGal has many potential applications in scientific experiments. It has been shown to be a useful tool for studying the biological functions of carbohydrates in biological systems. Additionally, it has been used as a substrate for enzymes that recognize galactose, and it has been used as a probe to study the interaction between carbohydrates and lectins.

Current state of research:

4FDGal is an area of active research in fields such as carbohydrate chemistry, molecular biology, and glycobiology. Many studies have focused on the synthesis, characterization, and biological properties of 4FDGal. Moreover, the use of 4FDGal in various scientific experiments is continually expanding.

Potential implications in various fields of research and industry:

The properties of 4FDGal make it an attractive tool for various fields of research and industry. It has potential applications in areas such as drug discovery, clinical diagnostics, and vaccine development. 4FDGal could also be used in the food industry as an artificial sweetener substitute.

Limitations and future directions:

There are some limitations associated with the use of 4FDGal, including its high cost and low availability. In addition, its toxicity profile is not yet fully understood. Future directions in research include exploring new methods for synthesizing 4FDGal, characterizing its biological properties more fully, and expanding the potential applications of 4FDGal.

Future directions:

There is potential to use 4FDGal in industrial, agricultural, and medical applications. There is potential to obtain clearer details about the structure of 4FDGal and its interaction with lectins and other enzymes. This might allow for the more targeted design of artificial sweeteners and drug discovery. Further research may also involve incorporating 4FDGal into polymers for potential use in constructing a more eco-friendly material. There is the potential for creating 4FDGal as a biosensor on a bio chip for quick medical tests as it has been noted as having characteristics suitable for this. Finally, there is potential in exploring the properties of 4FDGal in bacterial binding studies.

CAS Number

40010-20-6

Product Name

4-Fluoro-4-deoxy-D-galactopyranose

IUPAC Name

(3R,4R,5R,6R)-5-fluoro-6-(hydroxymethyl)oxane-2,3,4-triol

Molecular Formula

C6H11FO5

Molecular Weight

182.15 g/mol

InChI

InChI=1S/C6H11FO5/c7-3-2(1-8)12-6(11)5(10)4(3)9/h2-6,8-11H,1H2/t2-,3+,4+,5-,6?/m1/s1

InChI Key

FIHYONSINSKFAH-SVZMEOIVSA-N

SMILES

C(C1C(C(C(C(O1)O)O)O)F)O

Synonyms

4-Deoxy-4-fluoro-D-galactopyranose;

Canonical SMILES

C(C1C(C(C(C(O1)O)O)O)F)O

Isomeric SMILES

C([C@@H]1[C@@H]([C@@H]([C@H](C(O1)O)O)O)F)O

CAS No: 40010-20-6 MDL No: MFCD00057524 Chemical Formula: C6H11FO5 Molecular Weight: 182.15

References: 1. Marcus DM, Westwood JH, Carbohydr. Res. 1971, Apr 17(2), 269-74

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