Structure Information
Structure

Compound Identification

SMILES

NC1=NC2=C(N=CN2C2OC(CO)C(O)C2O)C(SC2=CC=C(C3=NON=C23)[N+]([O-])=O)=N1

InChIKey

InChIKey=KPNFSARMBBISMK-UHFFFAOYSA-N

Formula

C16H14N8O7S

Mass

462.4

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 - Diarylthioether - Pentose monosaccharide - 6-thiopurine - Benzoxadiazole - Imidazopyrimidine - Purine - Aryl thioether - Thiophenol ether - Nitroaromatic compound - Aminopyrimidine - N-substituted imidazole - Monosaccharide - Benzenoid - Pyrimidine - Oxadiazole - Oxolane - Azole - Imidazole - Furazan - Heteroaromatic compound - Secondary alcohol - C-nitro compound - Organic nitro compound - Thioether - Sulfenyl compound - Azacycle - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Oxacycle - Organoheterocyclic compound - Organic oxoazanium - Organic salt - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Amine - Primary alcohol - Primary amine - Organic nitrogen compound - Organic oxygen compound - Alcohol - Organic oxide - Organic zwitterion - 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

Previous Back Next