Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1C[C@H](O[C@H]1CO[P+](=O)O[P+](=O)O[P+](=O)O[P+](=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(=O)NC1=O)N1C=NC2=C1NC=NC2=S

InChIKey

InChIKey=VQEHTPWQSAISCP-GLHFQTAYSA-P

Formula

C19H22N6O16P4S

Mass

746.36

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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 - Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Purinethione - Imidazopyrimidine - Purine - Pyrimidone - Pyrimidinethione - Hydropyrimidine - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - 1,2-diol - Secondary alcohol - Urea - Lactam - Azacycle - Organoheterocyclic compound - Oxacycle - Organosulfur compound - Organooxygen compound - Hydrocarbon derivative - Alcohol - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organic nitrogen compound - 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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