Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2C1OC(CO)C2OP([O-])(=S)OC12

InChIKey

InChIKey=OMSUUENXGWGOLC-UHFFFAOYSA-M

Formula

C10H11N5O5PS

Mass

344.26

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

2',3'-cyclic purine nucleoside phosphorothioates

Intermediate Tree Nodes

Not available

Direct Parent

2',3'-cyclic purine nucleoside phosphorothioates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

2',3'-cyclic purine nucleoside phosphorothioate - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - Primary aromatic amine - Pyrimidine - Organic thiophosphoric acid or derivatives - Thiophosphoric acid ester - Imidolactam - Monosaccharide - N-substituted imidazole - Azole - Oxolane - 1,3_dioxaphospholane - Imidazole - Heteroaromatic compound - Oxacycle - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Primary amine - Primary alcohol - Organic anion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 2',3'-cyclic purine nucleoside phosphorothioates. These are 2',3'-cyclic purine nucleoside phosphate analogues, where a phosphate oxygen has been exchanged for sulphur generating a chiral phosphorothioate. In 2',3'-cyclic nucleoside phosphorothioate, the oxygen atoms at the 2'- and 3'-positions of the ribose are part of the phosphorothioate group.

External Descriptors

Not available

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