Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@@H](CO[P+](O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1NC(Cl)=NC2=O

InChIKey

InChIKey=TWGCJCNHCWBHID-UUOKFMHZSA-P

Formula

C10H11ClN4O7P

Mass

365.64

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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 - N-glycosyl compound - Glycosyl compound - 6-oxopurine - Pentose monosaccharide - Hypoxanthine - Imidazopyrimidine - Purine - Halopyrimidine - Pyrimidone - 2-halopyrimidine - Pyrimidine - Monosaccharide - N-substituted imidazole - Aryl chloride - Aryl halide - Azole - Heteroaromatic compound - Imidazole - Vinylogous amide - Oxolane - 1,2-diol - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Organohalogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organochloride - Organonitrogen compound - Organooxygen compound - Organic oxygen 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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