17659-59-5 Usage
Chemical compound
1,5-anhydroglucitol-6-phosphate is a chemical compound that plays a crucial role in energy metabolism and glucose regulation in the body.
Derivative
It is a derivative of 1,5-anhydro-D-glucitol, a naturally occurring sugar alcohol found in food sources such as wheat, rice, and corn.
Intermediate in glucose breakdown
1,5-anhydroglucitol-6-phosphate is an intermediate in the breakdown of glucose.
Key regulator of glucose homeostasis
1,5-anhydroglucitol-6-phosphate acts as a key regulator of glucose homeostasis, helping to control blood sugar levels and insulin sensitivity.
Potential role in diabetes
It is being studied for its potential role in the diagnosis and management of diabetes.
Potential as a biomarker
1,5-anhydroglucitol-6-phosphate has potential as a biomarker for kidney function.
Check Digit Verification of cas no
The CAS Registry Mumber 17659-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,5 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17659-59:
(7*1)+(6*7)+(5*6)+(4*5)+(3*9)+(2*5)+(1*9)=145
145 % 10 = 5
So 17659-59-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H13O8P/c7-3-1-13-4(6(9)5(3)8)2-14-15(10,11)12/h3-9H,1-2H2,(H2,10,11,12)/t3-,4+,5+,6+/m0/s1
17659-59-5Relevant articles and documents
A short and efficient synthesis of 1,5-anhydro-d-glucitol 6-phosphate
Yuan, Changyou,Hollingsworth, Rawle I.
, p. 5421 - 5423 (2011/10/31)
The important d-glucose and d-glucose 6-phosphate analogues 1,5-anhydro-d-glucitol and 1,5-anhydro-d-glucitol 6-phosphate were prepared from methyl-d-glucoside in high yield and purity. Protecting of the hydroxyl groups as their allyl ether followed by reductive cleavage of the glycosidic linkage with triethylsilane formed the protected anhydroglucitol. No ring rearrangement or ring contraction was observed during the reduction step. Using the PdCl 2-CuCl2-activated charcoal system, the allyl ether bond was cleaved with a low loading of the catalyst (0.0025 equiv per allyl group). 1,5-Anhydro-d-glucitol 6-phosphate was prepared by the phosphylation of 1,5-anhydro-d-glucitol.
