Compound Identification
SMILES
CCCNC1=NC2=C(N=CN=C2SCC2=CC=CC=C2)N1C1OC(CO)C(O)C1O
InChIKey
InChIKey=SQDWHYNKFJICLC-UHFFFAOYSA-N
Formula
C20H25N5O4S
Mass
431.51
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
Glycosylamines 6-thiopurines Pentoses Secondary alkylarylamines Alkylarylthioethers Pyrimidines and pyrimidine derivatives N-substituted imidazoles Aminoimidazoles Benzene and substituted derivatives Oxolanes Heteroaromatic compounds 1,2-diols Secondary alcohols Sulfenyl compounds Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - 6-thiopurine - Imidazopyrimidine - Purine - Aryl thioether - Secondary aliphatic/aromatic amine - Alkylarylthioether - Aminoimidazole - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Azole - Imidazole - Oxolane - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Sulfenyl compound - Azacycle - Organoheterocyclic compound - Secondary amine - Thioether - Oxacycle - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Alcohol - Primary 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