Compound Identification
SMILES
CC1(C)OC2C(CO)OC(C2O1)N1C=NC2=C1N=CN=C2SCC1=CC=CC=C1
InChIKey
InChIKey=QJAHUIXGBWOONU-UHFFFAOYSA-N
Formula
C20H22N4O4S
Mass
414.48
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Purine nucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Purine nucleosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Purine nucleosides
Alternative Parents
6-thiopurines Ketals Alkylarylthioethers Pyrimidines and pyrimidine derivatives N-substituted imidazoles Monosaccharides Benzene and substituted derivatives Tetrahydrofurans Heteroaromatic compounds 1,3-dioxolanes Sulfenyl compounds Oxacyclic compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - 6-thiopurine - Purine - Imidazopyrimidine - Aryl thioether - Ketal - Alkylarylthioether - Benzenoid - Pyrimidine - N-substituted imidazole - Monosaccharide - Monocyclic benzene moiety - Heteroaromatic compound - Tetrahydrofuran - Imidazole - Azole - Meta-dioxolane - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors
Not available