Structure Information
Structure

Compound Identification

SMILES

OC[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)N1C=NC2=CN=C(SC(=O)C3=CC=C(C=C3)[N+]([O-])=O)N=C12

InChIKey

InChIKey=QRQAGQIWMMOSBL-ABHRYQDASA-N

Formula

C17H15N5O7S

Mass

433.4

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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 - Benzoic acid or derivatives - Imidazopyrimidine - Nitrobenzene - Purine - Thiobenzoic acid or derivatives - Aryl thioether - Nitroaromatic compound - Benzoyl - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Imidazole - Heteroaromatic compound - Azole - Oxolane - 1,2-diol - Carbothioic s-ester - Thiocarboxylic acid ester - Secondary alcohol - C-nitro compound - Organic nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Sulfenyl compound - Thiocarboxylic acid or derivatives - Organoheterocyclic compound - Oxacycle - Organic oxoazanium - Azacycle - Organic nitrogen compound - Organic zwitterion - Alcohol - Organic oxygen compound - Organic salt - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Primary alcohol - 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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