Structure Information
Structure

Compound Identification

SMILES

OC[C@@H](O)[C@@H](O)[C@@H](O)C=O.OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(O)ncnc12.OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(O)nc(=N)[nH]c12

InChIKey

InChIKey=LCEITZUCKBLDQA-UHGLNUFFSA-N

Formula

C25H35N9O15

Mass

701.603

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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 - N-glycosyl compound - Glycosyl compound - Hypoxanthine - 6-oxopurine - Purine - Imidazopyrimidine - Hydroxypyrimidine - Pyrimidone - Pyrimidine - N-substituted imidazole - Monosaccharide - Beta-hydroxy aldehyde - Heteroaromatic compound - Vinylogous amide - Alpha-hydroxyaldehyde - Tetrahydrofuran - Imidazole - Azole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Primary alcohol - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aldehyde - 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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