Structure Information
Structure

Compound Identification

SMILES

COC1C(OP([O-])(=S)OCC2OC(CC2O)N2C=NC3=C2N=CN=C3N)C(CO)OC1N1C=CC(=O)NC1=O

InChIKey

InChIKey=LYMICVBGNUEHGE-UHFFFAOYSA-M

Formula

C20H25N7O10PS

Mass

586.49

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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 2'-deoxyribonucleoside - Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Monosaccharide - N-substituted imidazole - Thiophosphoric acid ester - Pyrimidine - Organic thiophosphoric acid or derivatives - Imidolactam - Azole - Oxolane - Vinylogous amide - Imidazole - Heteroaromatic compound - Urea - Secondary alcohol - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Dialkyl ether - Ether - Primary amine - Primary alcohol - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic anion - 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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