Structure Information
Structure

Compound Identification

SMILES

OP(O)(O)=O.N[C@@H](CO)C(=O)[C@]1(O[C@H](CO)[C@@H](O)[C@H]1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=WIMGDVVHRHFIJS-HRVUDFJESA-N

Formula

C13H21N6O10P

Mass

452.317

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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 - C-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Amino saccharide - Monosaccharide - N-substituted imidazole - Beta-hydroxy ketone - Organic phosphoric acid derivative - Imidolactam - Pyrimidine - Alpha-aminoketone - Azole - Heteroaromatic compound - Imidazole - Oxolane - Ketone - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Primary aliphatic amine - Organonitrogen compound - Organooxygen compound - Primary alcohol - Carbonyl group - Primary amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Amine - Organic oxygen 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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