Structure Information
Structure

Compound Identification

SMILES

CS(=O)(C[C@H](N)C(O)=O)=NP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=QISBAEFKTWAZEY-XPSMFXCBSA-N

Formula

C14H22N7O9PS

Mass

495.4

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic oxygen compounds

Class

Organooxygen compounds

Subclass

Carbohydrates and carbohydrate conjugates

Intermediate Tree Nodes

Glycosyl compounds

Direct Parent

Glycosylamines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

N-glycosyl compound - 6-aminopurine - Alpha-amino acid - Alpha-amino acid or derivatives - L-alpha-amino acid - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Imidolactam - Organic phosphoric acid derivative - Pyrimidine - Phosphoric acid ester - Azole - Heteroaromatic compound - Imidazole - Carbo-azosulfone - Oxolane - Secondary alcohol - Amino acid - Amino acid or derivatives - 1,2-diol - Organoheterocyclic compound - Azacycle - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid - Carboxylic acid derivative - Primary amine - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Amine - Organonitrogen compound - Organosulfur compound - Primary aliphatic amine - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).

External Descriptors

Not available

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