Structure Information
Structure

Compound Identification

SMILES

CNC1=NC=NC2=C1N=CN2[C@H]1C[C@H](O)[C@@H](CO[P+](=O)OP(O)(=O)O[P+](O)=O)O1

InChIKey

InChIKey=SPKQTCGMOUFFPJ-XLPZGREQSA-P

Formula

C11H16N5O10P3

Mass

471.194

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Deoxyribo- and ribonucleoside phosphonates

Subclass

Purine ribonucleoside phosphonates

Intermediate Tree Nodes

Not available

Direct Parent

Purine ribonucleoside phosphonates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside phosphonate - Purine 2'-deoxyribonucleoside - Purine nucleoside - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - N-substituted imidazole - Organic phosphoric acid derivative - Pyrimidine - Imidolactam - Heteroaromatic compound - Oxolane - Azole - Imidazole - Secondary alcohol - Azacycle - Organoheterocyclic compound - Oxacycle - Secondary amine - Organic oxygen compound - Amine - Alcohol - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside phosphonates. These are n-glycosyl compound that possess both a purine nucleobase linked to either a ribose or deoxyribose, which in turn carries a phosphonate group at the 5'-position.

External Descriptors

Not available

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