Structure Information
Structure

Compound Identification

SMILES

NC1=NC2=C(N=CN2C2OC(CO)C(O)C2O)C(SCC2=CC=C(Cl)C=C2)=N1

InChIKey

InChIKey=XQGREBVLUUSQLF-UHFFFAOYSA-N

Formula

C17H18ClN5O4S

Mass

423.87

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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 - Pentose monosaccharide - 6-thiopurine - Imidazopyrimidine - Purine - Aryl thioether - Halobenzene - Chlorobenzene - Alkylarylthioether - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Monocyclic benzene moiety - Aryl halide - Aryl chloride - Benzenoid - Pyrimidine - Imidazole - Azole - Heteroaromatic compound - Tetrahydrofuran - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Thioether - Sulfenyl compound - Organopnictogen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organosulfur compound - Alcohol - Primary alcohol - Primary amine - Organic oxygen compound - Amine - Hydrocarbon derivative - 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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