Structure Information
Structure

Compound Identification

SMILES

[H]C1(CO)OC([H])(N2C=CC(O)=NC2=O)C2([H])OP(O)(=S)OC12[H]

InChIKey

InChIKey=OIDQHQCLWHMGIL-UHFFFAOYSA-N

Formula

C9H11N2O7PS

Mass

322.23

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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 pyrimidine nucleoside phosphorothioates

Intermediate Tree Nodes

Not available

Direct Parent

2',3'-cyclic pyrimidine nucleoside phosphorothioates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

2',3'-cyclic pyrimidine nucleoside phosphorothioate - Hydroxypyrimidine - Pyrimidone - Thiophosphate diester - Hydropyrimidine - Monosaccharide - Thiophosphoric acid ester - Pyrimidine - Organic thiophosphoric acid or derivatives - 1,3_dioxaphospholane - Oxolane - Heteroaromatic compound - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 2',3'-cyclic pyrimidine nucleoside phosphorothioates. These are 2',3'-cyclic pyrimidine 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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