Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)C2=C(N1)N([C@H]1C[C@H](O)[C@@H](CO[P+](O)=O)O1)C(=O)N2

InChIKey

InChIKey=GPNDFUPZYFHVBB-VPENINKCSA-P

Formula

C10H13N5O7P

Mass

346.215

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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-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Vinylogous amide - Oxolane - Heteroaromatic compound - Urea - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Hydrocarbon derivative - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Organic nitrogen compound - Organic oxygen compound - Alcohol - 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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