Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@H]1C[C@H](N=[N+]=[N-])[C@@H](CO[P+](O)=O)O1

InChIKey

InChIKey=DUZQZOZHWRVJDD-RRKCRQDMSA-O

Formula

C10H12N8O4P

Mass

339.231

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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',3'-dideoxyribonucleoside - Purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Imidolactam - Pyrimidine - Primary aromatic amine - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Oxolane - Azo compound - Azo imide - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Primary amine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Amine - Organic salt - 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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