Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO[P+](O)([O-])OP(O)(=O)O[P+](O)(O)[O-])[C@@H](O)[C@H]1OC(=O)CCCCCN(C1=CC=CC2=NON=C12)[N+](O)=O

InChIKey

InChIKey=SOKVDGXBNRIMKC-RCAWKPMRSA-O

Formula

C22H29N9O17P3

Mass

784.441

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Benzoxadiazole - Imidazopyrimidine - Purine - Phenylhydrazine - Aminopyrimidine - Fatty acid ester - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Fatty acyl - Imidolactam - Pyrimidine - Benzenoid - Azole - Oxolane - Oxadiazole - Nitramine - Furazan - Imidazole - Heteroaromatic compound - Amino acid or derivatives - Organic nitro compound - Secondary alcohol - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Oxacycle - Organic salt - Primary amine - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Amine - Carbonyl group - Organic oxide - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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