thumb|120px|Cyclic hemiaminal ether bond derived from an aldehyde
Glycosylamines are a class of biochemical compounds consisting of a glycosyl group attached to an amino group, -NR<sub>2</sub>. They are also known as N-glycosides, as they are a type of glycoside. Glycosyl groups can be derived from carbohydrates. The glycosyl group and amino group are connected with a β-N-glycosidic bond, forming a cyclic hemiaminal ether bond (α-aminoether).
Examples include nucleosides such as adenosine.
Roles of Glycosylamines
Glycosylamine has many roles in biochemistry, such as synthesis in pharmaceutical compounds and forming enzymes, but one of the most important is to play as intermediates in biosignaling.
Carbohydrates function in important biological events, such as glycolysis, signal transduction, and other biochemical pathways. Glycosylamine is a sugar-related derivative where the anomeric oxygen of Glycoside has been replaced by nitrogen. They are specifically known for being small N-glycosyl mimics of glycosides,
A Schiff base can rearrange into an Amadori rearrangement compound, which is a more stable compound. The molecules that are a part of this arrangement can exist as glycosylamines or open-chain Schiff bases, and they get converted to 1-deoxy-2-keto-sugar derivatives primarily through N-glycosylamino acids.
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|thumb|150px|left|The nucleoside adenosine
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