Compound Identification
SMILES
C[C@@]1(O)[C@H](O)[C@@H](CO)OC1N1C=NC2=C1N=CN=C2N(O)C(=O)NC1=CC=CC=C1
InChIKey
InChIKey=LEVSNNFRTLBLQE-OQZUNHGWSA-N
Formula
C18H20N6O6
Mass
416.394
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 N-phenylureas Purines and purine derivatives Imidolactams Pyrimidines and pyrimidine derivatives Monosaccharides N-substituted imidazoles Tertiary alcohols Heteroaromatic compounds Oxolanes Secondary alcohols 1,2-diols Azacyclic compounds Oxacyclic compounds Carbonyl compounds Primary alcohols Hydrocarbon derivatives Organic oxides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - N-glycosyl compound - Glycosyl compound - N-phenylurea - Imidazopyrimidine - Purine - N-substituted imidazole - Imidolactam - Benzenoid - Pyrimidine - Monosaccharide - Monocyclic benzene moiety - Heteroaromatic compound - Imidazole - Tertiary alcohol - Oxolane - Azole - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - 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