39217-32-8 Usage
Uses
Used in Pharmaceutical Industry:
D-5-ketofructose 1,6-biphosphate is used as a pharmaceutical agent for the treatment of metabolic diseases such as diabetes. Its involvement in the regulation of glucose metabolism makes it a potential therapeutic target for managing blood sugar levels and improving insulin sensitivity.
Used in Research and Development:
D-5-ketofructose 1,6-biphosphate is used as a research tool in the study of glycolysis and its role in various metabolic processes. It helps scientists understand the mechanisms of glucose breakdown and energy production, as well as the factors that influence the activity of enzymes involved in the pathway.
Used in Biochemical Analysis:
D-5-ketofructose 1,6-biphosphate is used as a biochemical marker in diagnostic tests to assess the activity of enzymes involved in glycolysis. Measuring its levels can provide insights into the functioning of the glycolytic pathway and the presence of metabolic disorders.
Used in Nutritional Supplements:
D-5-ketofructose 1,6-biphosphate can be used as a nutritional supplement to support energy production and promote overall metabolic health. Its role in the glycolysis pathway may help enhance the body's ability to generate ATP and maintain optimal energy levels.
Check Digit Verification of cas no
The CAS Registry Mumber 39217-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,1 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 39217-32:
(7*3)+(6*9)+(5*2)+(4*1)+(3*7)+(2*3)+(1*2)=118
118 % 10 = 8
So 39217-32-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O12P2/c7-3(1-17-19(11,12)13)5(9)6(10)4(8)2-18-20(14,15)16/h5-6,9-10H,1-2H2,(H2,11,12,13)(H2,14,15,16)/t5-,6-/m1/s1
39217-32-8Relevant academic research and scientific papers
Butera, Loredana,Englard, Sasha,Blanchard, John S.,Avigad, Gad
, p. 179 - 188 (1986)
The mono- (2) and bis-phosphate (3) derivatives of D-threo-2,5-hexodiulose (1) (5-keto-D-fructose) were synthesized enzymically and purified by anion-exchange chromatography.The proportions, sizes of ring, and anomeric configurations were determined by F.t. 31P- and 13C-n.m.r. spectroscopy.Compound 2 was found to exist preponderantly (70-78percent) in the β-pyranose form with the remainder existing in the 2R,5R-furanose form.Compound 3 assumes two different furanose forms in solution, one (77-84percent) being the 2R,5R-furanose form and the other the 2S,5R-furanose form.
