Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2C1OC(COC(=O)C2=CN=CC=C2)C(O)C1O

InChIKey

InChIKey=VGCXTXVOZXMMDR-UHFFFAOYSA-N

Formula

C16H16N6O5

Mass

372.341

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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 - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - 6-aminopurine - Pyridine carboxylic acid or derivatives - Pyridine carboxylic acid - Purine - Imidazopyrimidine - Aminopyrimidine - Imidolactam - Pyrimidine - Pyridine - N-substituted imidazole - Monosaccharide - Heteroaromatic compound - Tetrahydrofuran - Imidazole - Azole - Secondary alcohol - Carboxylic acid ester - Amino acid or derivatives - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - 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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