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Structure Information
Structure

Compound Identification

SMILES

OC[C@@H]1O[C@H](C[C@H]1OP(O)(=S)OC[C@@H]1O[C@H](C[C@@H]1O)N1C=C(F)C(=O)NC1=O)N1C=C(F)C(=O)NC1=O

InChIKey

InChIKey=DOYINWDAMLUPNA-HOEOXQICSA-N

Formula

C18H21F2N4O11PS

Mass

570.41

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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 2'-deoxyribonucleoside - Pyrimidine nucleoside - Halopyrimidine - Pyrimidone - Thiophosphate diester - Aryl fluoride - Aryl halide - Hydropyrimidine - Thiophosphoric acid ester - Pyrimidine - Organic thiophosphoric acid or derivatives - Vinylogous amide - Heteroaromatic compound - Oxolane - Urea - Secondary alcohol - Lactam - Azacycle - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Organonitrogen compound - Organofluoride - Organohalogen compound - Organooxygen compound - Primary alcohol - Alcohol - Organic oxygen compound - Organic oxide - Organic nitrogen compound - 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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