Structure Information
Structure

Compound Identification

SMILES

NC1=NC(F)=NC2=C1N=CN2C1OC(CO)C(O)C1O.NC1=NC(F)=NC2=C1N=CN2C1OC(COC=O)C(O)C1O.NC1=NC(F)=NC2=C1N=CN2C1OC(COC=O)C(OC=O)C1O.NC1=NC(F)=NC2=C1N=CN2C1OC(COC=O)C(O)C1OC=O

InChIKey

InChIKey=NNMUEDWQXBJISJ-UHFFFAOYSA-N

Formula

C45H48F4N20O21

Mass

1280.992

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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

Not available

Substituents

Purine nucleoside - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - 2-halopyrimidine - Aminopyrimidine - Halopyrimidine - Monosaccharide - N-substituted imidazole - Aryl fluoride - Aryl halide - Dicarboxylic acid or derivatives - Pyrimidine - Imidolactam - Imidazole - Azole - Heteroaromatic compound - Oxolane - Amino acid or derivatives - Carboxylic acid ester - Secondary alcohol - Oxacycle - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Primary alcohol - Primary amine - Organic oxygen compound - Amine - Carbonyl group - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - 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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