Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=S)O[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O

InChIKey

InChIKey=YJOLYRGOINBELN-FBFQDNEDSA-N

Formula

C20H25N10O9PS

Mass

612.51

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

(3'->5')-dinucleotides and analogues

Subclass

(3'->5')-dinucleotide phosphorothioates

Intermediate Tree Nodes

Not available

Direct Parent

(3'->5')-dinucleotide phosphorothioates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

(3'->5')-dinucleotide phosphorothioate - Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - Thiophosphate diester - Imidolactam - Organic thiophosphoric acid or derivatives - Pyrimidine - Monosaccharide - N-substituted imidazole - Thiophosphoric acid ester - Heteroaromatic compound - Azole - Imidazole - Oxolane - 1,2-diol - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Azacycle - Primary alcohol - Primary amine - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Amine - Alcohol - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as (3'->5')-dinucleotide phosphorothioates. These are compounds consisting of two ribose moieties connected one 5',3'-phosphomonothioic acid O,O'-diester bond. Each ribose unit is N-linked to a nucleic base or an analogue thereof.

External Descriptors

Not available

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