Compound Identification
SMILES
C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1N1C=NC2=C(N=CN=C12)C1=CC=CC(=C1)C#N
InChIKey
InChIKey=MITKZLBMFOBRQV-DGCUDZEOSA-N
Formula
C18H17N5O4
Mass
367.365
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
Phenylpyrimidines Glycosylamines Purines and purine derivatives Benzonitriles N-substituted imidazoles Monosaccharides Tertiary alcohols Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Azacyclic compounds Oxacyclic compounds Nitriles Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - 4-phenylpyrimidine - Glycosyl compound - N-glycosyl compound - Imidazopyrimidine - Purine - Benzonitrile - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Benzenoid - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Tertiary alcohol - 1,2-diol - Secondary alcohol - Nitrile - Carbonitrile - Azacycle - Oxacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Cyanide - Organic oxygen compound - Primary alcohol - Organic nitrogen 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