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Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](CO[P+](=O)O[C@@H](C2=CC=CO2)P(O)(O)=O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=ANIYCXQAWZLMKX-JOLIMNQDSA-O

Formula

C14H18N3O11P2

Mass

466.255

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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 heteromonocyclic compounds

Substituents

Purine ribonucleoside phosphonate - Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Imidolactam - Furan - Organophosphonic acid - Organophosphonic acid derivative - Oxolane - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Amine - Organic nitrogen compound - Organonitrogen compound - Alcohol - Organooxygen compound - Organic oxide - Organic oxygen compound - Organophosphorus compound - Primary amine - Organic cation - Aromatic heteromonocyclic 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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