Structure Information
Structure

Compound Identification

SMILES

NC1=NC(N\N=C\C=C\C2=CC=CC=C2[N+]([O-])=O)=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

InChIKey

InChIKey=OQHQDJKKAVBZKY-VWSCUNPCSA-N

Formula

C19H20N8O6

Mass

456.419

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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 - Pentose monosaccharide - 6-aminopurine - Nitrobenzene - Imidazopyrimidine - Purine - Nitroaromatic compound - Styrene - Aminopyrimidine - Monosaccharide - Imidolactam - Monocyclic benzene moiety - Pyrimidine - Benzenoid - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Oxolane - 1,2-diol - Organic nitro compound - C-nitro compound - Secondary alcohol - Organoheterocyclic compound - Hydrazone - Oxacycle - Azacycle - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Amine - Alcohol - Organic oxygen 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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