6866-69-9 Usage
Description
N-acetylglucosamine-1-phosphate, also known as NAG-1-P, is a modified sugar molecule derived from N-acetyl-D-glucosamine. It is characterized by the presence of a phosphate group at the first carbon position and an acetamido group at the second carbon position. N-acetylglucosamine-1-phosphate plays a crucial role in various biological processes and serves as an important intermediate in the biosynthesis of glycoconjugates and other complex carbohydrates.
Uses
Used in Pharmaceutical Industry:
N-acetylglucosamine-1-phosphate is used as a key intermediate in the synthesis of various pharmaceutical compounds, such as antibiotics, antifungals, and antiviral agents. Its unique structure allows for the development of novel drugs with improved efficacy and reduced side effects.
Used in Biotechnology:
In the biotechnology field, N-acetylglucosamine-1-phosphate is utilized as a building block for the production of complex carbohydrates, glycoproteins, and other bioactive molecules. These molecules have potential applications in drug discovery, vaccine development, and the creation of biomaterials for tissue engineering.
Used in Nutritional Supplements:
N-acetylglucosamine-1-phosphate is used as an ingredient in nutritional supplements, particularly those aimed at promoting joint health and supporting the immune system. Its role in the synthesis of glycosaminoglycans, which are essential components of cartilage and other connective tissues, makes it a valuable addition to these products.
Used in Research and Development:
N-acetylglucosamine-1-phosphate is an important compound for researchers studying various aspects of cellular metabolism, carbohydrate biosynthesis, and the role of sugar molecules in cellular signaling. It serves as a valuable tool for understanding the mechanisms underlying various diseases and for developing targeted therapeutic strategies.
Used in Cosmetics Industry:
In the cosmetics industry, N-acetylglucosamine-1-phosphate is used as an active ingredient in skincare products due to its potential benefits for skin health. It is believed to promote the synthesis of hyaluronic acid, a key component of the skin's extracellular matrix, which helps maintain skin hydration and elasticity.
Check Digit Verification of cas no
The CAS Registry Mumber 6866-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,6 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6866-69:
(6*6)+(5*8)+(4*6)+(3*6)+(2*6)+(1*9)=139
139 % 10 = 9
So 6866-69-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H16NO9P/c1-3(11)9-5-7(13)6(12)4(2-10)17-8(5)18-19(14,15)16/h4-8,10,12-13H,2H2,1H3,(H,9,11)(H2,14,15,16)/t4-,5-,6-,7-,8?/m1/s1
6866-69-9Relevant articles and documents
Wide sugar substrate specificity of galactokinase from Streptococcus pneumoniae TIGR4
Chen, Min,Chen, Lei-Lei,Zou, Yang,Xue, Mengyang,Liang, Min,Jin, Lan,Guan, Wan-Yi,Shen, Jie,Wang, Wenjun,Wang, Lei,Liu, Jun,Wang, Peng George
, p. 2421 - 2425 (2011)
Galactokinases (GALK) have attracted significant research attention for their potential application in the enzymatic synthesis of unique sugar phosphates. The galactokinase (GalKSpe4) cloned from Streptococcus pneumoniae TIGR4 had a temperature optimum of 45 °C, and a pH optimum of 8.0. The substrate specificity and kinetics studies revealed that GalKSpe4 had moderate activity toward glucose, in contrast with very low or no activity observed in other previously reported GALKs. Most interestingly, GalKSpe4 exhibited activity for GalNAc, which had never been recorded in other GALKs found by now. This is the first time to report that bacterial GALK can recognize GalNAc.
