Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](CO)[C@@H](OP(O)(=S)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(=O)NC2=O)[C@H]1O

InChIKey

InChIKey=VZQLNJPTHATNOF-IVQUQKRUSA-N

Formula

C18H24N5O12PS

Mass

565.45

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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 heteromonocyclic compounds

Substituents

(3'->5')-dinucleotide phosphorothioate - Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Aminopyrimidine - Pyrimidone - Thiophosphate diester - Hydropyrimidine - Monosaccharide - Thiophosphoric acid ester - Pyrimidine - Imidolactam - Organic thiophosphoric acid or derivatives - Heteroaromatic compound - Oxolane - Vinylogous amide - Urea - Secondary alcohol - Lactam - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Primary amine - Organonitrogen compound - Organooxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Amine - Primary alcohol - Aromatic heteromonocyclic 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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