Structure Information
Structure

Compound Identification

SMILES

NC1=NC(N=NC2=CC=CC=C2)=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@H](O)C1O

InChIKey

InChIKey=DXVZIROMNKAGQJ-WABSSEDKSA-N

Formula

C16H17N7O4

Mass

371.357

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monocyclic benzene moiety - Imidolactam - Monosaccharide - Benzenoid - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Oxolane - 1,2-diol - Azo compound - Secondary alcohol - Azacycle - Oxacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Primary alcohol - Primary amine - Organooxygen compound - Organic oxygen compound - Alcohol - Amine - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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