Compound Identification
SMILES
[H]C1(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)SC([H])(N2C=CC(=N)N=C2O)C([H])(O)C1([H])O
InChIKey
InChIKey=OHINSMXJPMRQOP-UHFFFAOYSA-N
Formula
C9H16N3O13P3S
Mass
499.22
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Nucleoside and nucleotide analogues
- Subclass Thionucleosides
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Class
Nucleoside and nucleotide analogues
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Thionucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Thionucleosides
Alternative Parents
Monoalkyl phosphates Hydroxypyrimidines Hydropyrimidines Thiolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Dialkylthioethers Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine thionucleoside - Hydroxypyrimidine - Monoalkyl phosphate - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Thiolane - Heteroaromatic compound - 1,2-diol - Secondary alcohol - Azacycle - Thioether - Organoheterocyclic compound - Dialkylthioether - Alcohol - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as thionucleosides. These are nucleoside analogues that contain a thiolane or a thietane that is 1,3-disubstituted with a hydroxyl group and pyrimidine or purine base, at the 1- and 3-position, respectively.
External Descriptors
Not available