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
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
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
Thiophosphate diesters Pyrimidones Hydroxypyrimidines Monosaccharides Hydropyrimidines Oxolanes Heteroaromatic compounds Dioxaphospholanes Oxacyclic compounds Azacyclic compounds Primary alcohols Organonitrogen compounds Organic oxides Hydrocarbon derivatives
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