32181-59-2 Usage
Chemical Properties
White Crystalline Solid
Uses
Different sources of media describe the Uses of 32181-59-2 differently. You can refer to the following data:
1. A component of oligosaccharide portion of many N- and O-linked glycoproteins. It is a building unit for the antigenic determinants of a number of certain human blood group activities as well as of the ABH Type 2 determinants
2. N-Acetyl-D-lactosamine is used as a specific lectin target molecule in the identification and differentiation of sugar binding molecules such as the galectins. N-Acetyl-D-lactosamine is used in studies of galactosidase, fucosyltransferase, sialyltransferase, and lectin inhibition.
3. N-Acetyllactosamine is used in the expansion of a multi-funcational natural scaffold for the study of structural space of the Galectin-1-Ligand interaction. Also, it is used to identify the impurity as an imidazoline ring structure.
Purification Methods
Purify N-acetyl-D-lactosamine by recrystallisation from MeOH (with 1 mol of MeOH) or from H2O. It is available commercially as a solution of 0.5g/mL of H2O. [Zilliken J Biol Chem 271 181 1955, Beilstein 17 IV 3452.]
Check Digit Verification of cas no
The CAS Registry Mumber 32181-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,8 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32181-59:
(7*3)+(6*2)+(5*1)+(4*8)+(3*1)+(2*5)+(1*9)=92
92 % 10 = 2
So 32181-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H25NO11/c1-4(18)15-7-9(20)12(6(3-17)24-13(7)23)26-14-11(22)10(21)8(19)5(2-16)25-14/h5-14,16-17,19-23H,2-3H2,1H3,(H,15,18)
32181-59-2Relevant articles and documents
Two-Step Chemoenzymatic Detection of N-Acetylneuraminic Acid-α(2-3)-Galactose Glycans
Wen, Liuqing,Zheng, Yuan,Jiang, Kuan,Zhang, Mingzhen,Kondengaden, Shukkoor Muhammed,Li, Shanshan,Huang, Kenneth,Li, Jing,Song, Jing,Wang, Peng George
supporting information, p. 11473 - 11476 (2016/10/07)
Sialic acids are typically linked α(2-3) or α(2-6) to the galactose that located at the non-reducing terminal end of glycans, playing important but distinct roles in a variety of biological and pathological processes. However, details about their respective roles are still largely unknown due to the lack of an effective analytical technique. Herein, a two-step chemoenzymatic approach for the rapid and sensitive detection of N-acetylneuraminic acid-α(2-3)-galactose glycans is described.