Structure Information
Structure

Compound Identification

SMILES

CC(=O)OCC1OC(C(OC(C)=O)C1OC(C)=O)N1C=NC2=C1N=C(F)N=C2NN

InChIKey

InChIKey=KRVXMBTUZVJXCQ-UHFFFAOYSA-N

Formula

C16H19FN6O7

Mass

426.361

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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 - N-glycosyl compound - Glycosyl compound - Tricarboxylic acid or derivatives - Purine - Imidazopyrimidine - 2-halopyrimidine - Halopyrimidine - Imidolactam - Pyrimidine - N-substituted imidazole - Monosaccharide - Aryl halide - Aryl fluoride - Heteroaromatic compound - Tetrahydrofuran - Imidazole - Azole - Carboxylic acid ester - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Hydrazine derivative - Carbonyl group - 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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