Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NCC1=CC(=CC=C1)[N+]([O-])=O

InChIKey

InChIKey=WZTYPOXBABAMJQ-LSCFUAHRSA-N

Formula

C17H18N6O6

Mass

402.367

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