Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@@H](COC2=CC=CC=C2F)O[C@H]([C@@H]1O)N1C=NC2=C1N=CN=C2N[C@@H]1CCOC1

InChIKey

InChIKey=QBYBDGUWZNPYIU-SEYPNCJNSA-N

Formula

C20H22FN5O5

Mass

431.424

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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-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Phenoxy compound - Phenol ether - Alkyl aryl ether - Aminopyrimidine - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Imidolactam - Monosaccharide - N-substituted imidazole - Benzenoid - Pyrimidine - Oxolane - Imidazole - Heteroaromatic compound - Azole - 1,2-diol - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Dialkyl ether - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Amine - 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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