6-Chloro-6-deoxy-D-glucose is a monosaccharide derivative of glucose, characterized by the substitution of a chlorine atom at the 6-position of the glucose molecule, resulting in the absence of the hydroxyl group typically found at this position. This modification imparts unique chemical properties to the compound, influencing its reactivity and biological interactions. The presence of the chlorine atom can affect the compound's solubility, stability, and potential as a substrate for enzymatic reactions. As a deoxy sugar, it lacks the hydroxyl group at the 6-position, which can alter its participation in glycosidic bond formation and its overall metabolic pathways. 6-Chloro-6-deoxy-D-glucose may be utilized in various biochemical research applications, particularly in studies involving carbohydrate metabolism and enzyme specificity. Its structural similarity to glucose allows it to be a useful tool in understanding the mechanisms of sugar transport and utilization in biological systems. However, due to its halogenated nature, it may also exhibit different biological activities compared to its parent compound, glucose.

6-Chloro-6-deoxy-D-glucose

40656-44-8: 6-Chloro-6-deoxy-D-glucose is a monosaccharide derivative of glucose, characterized by the substitution of a chlorine atom at the 6-position of the glucose molecule, resulting in the absence of the hydroxyl group typically found at this position. This modification imparts unique chemical properties to the compound, influencing its reactivity and biological interactions. The presence of the chlorine atom can affect the compound's solubility, stability, and potential as a substrate for enzymatic reactions. As a deoxy sugar, it lacks the hydroxyl group at the 6-position, which can alter its participation in glycosidic bond formation and its overall metabolic pathways. 6-Chloro-6-deoxy-D-glucose may be utilized in various biochemical research applications, particularly in studies involving carbohydrate metabolism and enzyme specificity. Its structural similarity to glucose allows it to be a useful tool in understanding the mechanisms of sugar transport and utilization in biological systems. However, due to its halogenated nature, it may also exhibit different biological activities compared to its parent compound, glucose.

<p>6-Chloro-6-deoxy-D-glucose is a sugar that is used as a carbon source in the process of spermatozoa production. It has been shown to increase the fertility of animals by increasing the uptake of phosphorus pentachloride and ganglion cells in the testes. This drug also has contraceptive and antifertility effects, which may be due to its ability to inhibit the uptake of adenine nucleotide in cells. 6-Chloro-6-deoxy-D-glucose may have a role in ATP levels, with intracellular levels being higher than those in control analysis.</p>

CAS 40656-44-8

6-Chloro-6-deoxy-D-glucose

6-Chloro-6-deoxy-D-glucose

Ref: 3D-MC146795