Methyl-2,3-dideoxy-3-fluoro-5-o-(4-phenylbenzoyl)-alpha-D-erythro-pentofuranoside is a synthetic carbohydrate derivative characterized by its unique structural features, including a furanose ring and specific functional groups. This compound contains a methyl group, a fluorine atom, and a phenylbenzoyl moiety, which contribute to its chemical reactivity and potential biological activity. The presence of the dideoxy and fluorine substituents suggests that it may exhibit altered properties compared to its parent sugars, potentially influencing its interaction with biological systems, such as enzymes or receptors. The phenylbenzoyl group may enhance lipophilicity, affecting solubility and permeability. This compound is of interest in medicinal chemistry and glycoscience, particularly for its potential applications in drug development or as a tool in biochemical research. Its specific stereochemistry, denoted by the alpha configuration, plays a crucial role in determining its biological interactions and overall functionality. As with many synthetic compounds, careful consideration of its stability, reactivity, and biological implications is essential for its application in research or therapeutic contexts.

methyl-2,3-dideoxy-3-fluoro-5-o-(4-phenylbenzoyl)-alpha-d-erythro-pentofuranoside

168786-98-9: Methyl-2,3-dideoxy-3-fluoro-5-o-(4-phenylbenzoyl)-alpha-D-erythro-pentofuranoside is a synthetic carbohydrate derivative characterized by its unique structural features, including a furanose ring and specific functional groups. This compound contains a methyl group, a fluorine atom, and a phenylbenzoyl moiety, which contribute to its chemical reactivity and potential biological activity. The presence of the dideoxy and fluorine substituents suggests that it may exhibit altered properties compared to its parent sugars, potentially influencing its interaction with biological systems, such as enzymes or receptors. The phenylbenzoyl group may enhance lipophilicity, affecting solubility and permeability. This compound is of interest in medicinal chemistry and glycoscience, particularly for its potential applications in drug development or as a tool in biochemical research. Its specific stereochemistry, denoted by the alpha configuration, plays a crucial role in determining its biological interactions and overall functionality. As with many synthetic compounds, careful consideration of its stability, reactivity, and biological implications is essential for its application in research or therapeutic contexts.

<p>A mutant is a modified form of a gene that can be either natural or artificial. This gene has been modified by the introduction of an additional chemical group, such as methyl, at a specific position in the DNA sequence. The new compound is not found in nature and may have beneficial effects on the organism. The control system for this experiment is programmable and allows for the introduction of multiple mutations to be introduced simultaneously into a single gene. This technique has been shown to create mutants with neurological disorders, including protein overload, which occurs when there are too many proteins made by one particular gene.</p>

CAS 168786-98-9

methyl-2,3-dideoxy-3-fluoro-5-o-(4-phenylbenzoyl)-alpha-d-erythro-pentofuranoside

Methyl-2,3-dideoxy-3-fluoro-5-O-(4-phenylbenzoyl)-a-D-erythro-pentofuranoside

Ref: 3D-MM31055