Structure Information
Structure

Compound Identification

SMILES

NC1=NC2=C(N=CN2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C(SCC2=CC=CC=C2[N+]([O-])=O)=N1

InChIKey

InChIKey=NYKLJFUOUDMWDF-XNIJJKJLSA-N

Formula

C17H18N6O6S

Mass

434.43

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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 - Nitrobenzene - Purine - Aryl thioether - Nitroaromatic compound - Aminopyrimidine - Alkylarylthioether - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Heteroaromatic compound - Imidazole - Oxolane - Azole - C-nitro compound - 1,2-diol - Organic nitro compound - Secondary alcohol - Allyl-type 1,3-dipolar organic compound - Thioether - Oxacycle - Sulfenyl compound - Organic oxoazanium - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Organic salt - Organonitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organic oxygen compound - Organosulfur compound - Primary alcohol - Primary amine - Organic nitrogen compound - Organic zwitterion - 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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