Structure Information
Structure

Compound Identification

SMILES

CCCCCCSC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(O)(O)=S)[C@@H](O)[C@H]2O)C(N)=N1

InChIKey

InChIKey=DPAGUSSBIWVODX-SDBHATRESA-N

Formula

C16H26N5O6PS2

Mass

479.51

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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 - Purine - Aryl thioether - Aminopyrimidine - Alkylarylthioether - Organic thiophosphoric acid or derivatives - Thiophosphate monoester - Thiophosphoric acid ester - Imidolactam - N-substituted imidazole - Pyrimidine - Monosaccharide - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - 1,2-diol - Thioether - Sulfenyl compound - Organoheterocyclic compound - Azacycle - Oxacycle - Organosulfur compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organic oxygen compound - Amine - Organooxygen compound - Primary amine - 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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