Compound Identification
SMILES
NC1=NC=NC2=C1N=CN2C1SC(CO)C(O)C1O.NC1=NC=NC2=C1N=CN2C1SC(CO)C(O)C1O
InChIKey
InChIKey=FDHWXWCOFKFESQ-UHFFFAOYSA-N
Formula
C20H26N10O6S2
Mass
566.61
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
6-aminopurines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Thiolanes Heteroaromatic compounds Secondary alcohols Dialkylthioethers Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Not available
Substituents
Purine thionucleoside - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - Imidolactam - Pyrimidine - N-substituted imidazole - Heteroaromatic compound - Thiolane - Imidazole - Azole - Secondary alcohol - Azacycle - Organoheterocyclic compound - Dialkylthioether - Thioether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - 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