Compound Identification
SMILES
COC1=NC(N)=NC2=C1N=CN2[C@H]1C[C@H](O)[C@@H](CO)S1
InChIKey
InChIKey=QCWJONZOOIDYSL-RRKCRQDMSA-N
Formula
C11H15N5O3S
Mass
297.33
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Nucleoside and nucleotide analogues
- Subclass Thionucleosides
-
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
Hypoxanthines Aminopyrimidines and derivatives Alkyl aryl ethers N-substituted imidazoles Thiolanes Heteroaromatic compounds Secondary alcohols Dialkylthioethers Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine thionucleoside - Hypoxanthine - Imidazopyrimidine - Purine - Alkyl aryl ether - Aminopyrimidine - N-substituted imidazole - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Thiolane - Secondary alcohol - Ether - Azacycle - Organoheterocyclic compound - Dialkylthioether - Thioether - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Aromatic heteropolycyclic 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