Compound Identification
SMILES
CC(CC1=CC=CC=C1)NC1=NC=NC2=C1N=CN2[C@@H]1OC(CO)C(O)[C@H]1O
InChIKey
InChIKey=RIRGCFBBHQEQQH-ZICQKSQMSA-N
Formula
C19H23N5O4
Mass
385.424
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-alkylaminopurines Glycosylamines Pentoses Amphetamines and derivatives Phenylpropanes Aminopyrimidines and derivatives Imidolactams N-substituted imidazoles Heteroaromatic compounds Oxolanes Secondary alcohols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Primary alcohols Amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Amphetamine or derivatives - Pentose monosaccharide - Purine - Imidazopyrimidine - Phenylpropane - Aminopyrimidine - Imidolactam - Benzenoid - Monocyclic benzene moiety - Pyrimidine - Monosaccharide - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Oxolane - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Primary alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Alcohol - Amine - Organonitrogen compound - Organooxygen 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