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Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(=S)O[C@H]3C[C@@H](O[C@@H]3CO)N3C=CC(N)=NC3=O)O2)C(=O)NC1=O

InChIKey

InChIKey=WCWBUCLHFXOEDH-PCYLLWSFSA-N

Formula

C19H26N5O10PS

Mass

547.48

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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 - Aminopyrimidine - Pyrimidone - Thiophosphate diester - Hydropyrimidine - Thiophosphoric acid ester - Pyrimidine - Organic thiophosphoric acid or derivatives - Imidolactam - Oxolane - Heteroaromatic compound - Vinylogous amide - Secondary alcohol - Urea - Lactam - Azacycle - Oxacycle - Organoheterocyclic compound - Organic nitrogen compound - Primary alcohol - Alcohol - Organooxygen compound - Organonitrogen compound - Organic oxide - Primary amine - Organic oxygen compound - Hydrocarbon derivative - Amine - 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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