Structure Information
Structure

Compound Identification

SMILES

CSC1=NC(=O)N(C=C1)[C@@H]1O[C@H](CO[P+](=O)O[P+](=O)O[P+](=O)OC[C@@H]2O[C@@H]([C@@H](O)[C@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O

InChIKey

InChIKey=SLJNSXPJOOCVSX-OJTRBPGDSA-N

Formula

C20H25N7O14P3S

Mass

712.43

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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 nucleoside - Pyrimidine nucleoside - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aryl thioether - Pyrimidone - Alkylarylthioether - Aminopyrimidine - Hydropyrimidine - Monosaccharide - N-substituted imidazole - Imidolactam - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - 1,2-diol - Thioether - Sulfenyl compound - Oxacycle - Organoheterocyclic compound - Azacycle - Primary amine - Amine - Organonitrogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Organosulfur 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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