Compound Identification
SMILES
CC1=CC(C)=C(NC2=NC=NC3=C2N=CN3C2OC(CO)C(O)C2O)C=C1
InChIKey
InChIKey=APQIAUXRPNCQAC-UHFFFAOYSA-N
Formula
C18H21N5O4
Mass
371.397
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-aminopurines Pentoses m-Xylenes Aniline and substituted anilines Aminopyrimidines and derivatives Imidolactams N-substituted imidazoles Heteroaromatic compounds Oxolanes 1,2-diols Secondary alcohols Azacyclic compounds Secondary amines Oxacyclic compounds Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - M-xylene - Xylene - Aniline or substituted anilines - Aminopyrimidine - Imidolactam - Benzenoid - Monocyclic benzene moiety - Pyrimidine - Monosaccharide - N-substituted imidazole - Azole - Imidazole - Heteroaromatic compound - Oxolane - 1,2-diol - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Secondary amine - Organonitrogen compound - Organic nitrogen compound - Alcohol - Organic oxygen compound - Organooxygen compound - Amine - Hydrocarbon derivative - 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