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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](C(O)=O)C2=CC=CC=C2)[C@@H](O)[C@H]1O

InChIKey

InChIKey=YOQAVERQDFZIHU-DVLUHMITSA-O

Formula

C17H19N3O9P

Mass

440.324

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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 - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Aminopyrimidine - Pyrimidone - Pyrimidine - Monosaccharide - Benzenoid - Imidolactam - Hydropyrimidine - Monocyclic benzene moiety - Oxolane - Heteroaromatic compound - Amino acid or derivatives - 1,2-diol - Amino acid - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic oxygen compound - Amine - Alcohol - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen 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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