کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1389591 | 982898 | 2009 | 7 صفحه PDF | دانلود رایگان |
Glycoconjugates can be readily formed by the condensation of a free-reducing terminus and a strong α-effect nucleophile, such as a hydrazide or a hydroxylamine. Further characterization of a series of glycoconjugates formed from xylose, glucose and N-acetylglucosamine, and either p-toluenesulfonyl hydrazide or an N-methylhydroxylamine, was carried out to gain insight into the optimal conditions for the formation of these useful conjugates, and their stability. Their apparent association constants (9–74 M−1) at pH 4.5; as well, as rate constants for hydrolysis, at pH 4.0, 5.0 and 6.0 (37 °C), were determined. The half-lives of the conjugates varied between 3 h and 300 days. All the compounds were increasingly stable as the pH approached neutrality. Conjugate hydrolysis rates mirrored those found for O-glycoside hydrolysis where conjugates formed from electron-rich monosaccharides hydrolyzed more rapidly.
Hydrazides and N-methylhydroxylamines are useful reagents for conjugation to unprotected mono- and oligosaccharides. Investigation of their association constants as well as their hydrolysis rates provides insight into their applicability.Figure optionsDownload as PowerPoint slide
Journal: Carbohydrate Research - Volume 344, Issue 3, 17 February 2009, Pages 278–284