Structure Information
Structure

Compound Identification

SMILES

OC[C@@H](O)[C@@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)C=O.NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

InChIKey

InChIKey=AVBDKCPHFVBWMP-LEHDZVBWSA-N

Formula

C15H25N5O15P2

Mass

577.333

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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

Not available

Substituents

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - Imidolactam - Monosaccharide - Alkyl phosphate - N-substituted imidazole - Pyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Azole - Imidazole - Oxolane - Heteroaromatic compound - 1,2-diol - Secondary alcohol - Azacycle - Oxacycle - Organoheterocyclic compound - Primary amine - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Amine - Alcohol - Aldehyde - Primary 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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