Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=HNRQCEZXCMMODB-UBEDBUPSSA-N

Formula

C16H16N6O6

Mass

388.34

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