Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(NCC1=CC=CC=C1)N=C2SCC1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=OZVVAXZRRDJZQV-ZDXOVATRSA-N

Formula

C24H24N6O6S

Mass

524.55

Export to:

JSON SDF CSV

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

Previous Back Next