Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COC[C@H](O)COC2=CC=CC3=CC=CC=C23)[C@@H](O)[C@H]1O

InChIKey

InChIKey=IBMUHUFMSBVMPF-KVXBPHRHSA-N

Formula

C23H25N5O6

Mass

467.482

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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 - Naphthalene - Pentose monosaccharide - Imidazopyrimidine - Purine - Alkyl aryl ether - Aminopyrimidine - Glycerol ether - Monosaccharide - N-substituted imidazole - Primary aromatic amine - Imidolactam - Benzenoid - Pyrimidine - Oxolane - Azole - Heteroaromatic compound - Imidazole - Secondary alcohol - Organoheterocyclic compound - Dialkyl ether - Ether - Azacycle - Oxacycle - Hydrocarbon derivative - Organopnictogen compound - Organooxygen compound - Primary amine - Organonitrogen compound - Amine - Organic oxygen compound - Organic nitrogen compound - 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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