Structure Information
Structure

Compound Identification

SMILES

CC(=O)OCC1OC(C(OC(C)=O)C1OC(C)=O)N1C=NC2=C1N=C(Cl)N=C2N

InChIKey

InChIKey=IMTFOTCIQPKKSP-UHFFFAOYSA-N

Formula

C16H18ClN5O7

Mass

427.8

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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 - 6-aminopurine - Imidazopyrimidine - Purine - Tricarboxylic acid or derivatives - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - N-substituted imidazole - Monosaccharide - Aryl chloride - Aryl halide - Pyrimidine - Imidolactam - Heteroaromatic compound - Azole - Tetrahydrofuran - Imidazole - Amino acid or derivatives - Carboxylic acid ester - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Primary amine - Organopnictogen compound - Organic oxygen compound - Amine - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organochloride - 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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