Compound Identification
SMILES
NCC1=NC2=C(N=CN2C2OC(CO)C(O)C2O)C(NCCC2=CC=CC=C2)=N1
InChIKey
InChIKey=MKYFLZJTCCEUSM-UHFFFAOYSA-N
Formula
C19H24N6O4
Mass
400.439
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 Aminopyrimidines and derivatives Aralkylamines Benzene and substituted derivatives Imidolactams N-substituted imidazoles Heteroaromatic compounds Oxolanes Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary alcohols Hydrocarbon derivatives Monoalkylamines Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - 6-alkylaminopurine - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Aralkylamine - Monocyclic benzene moiety - Monosaccharide - Imidolactam - Benzenoid - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Imidazole - Oxolane - Azole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Primary aliphatic amine - Primary amine - Amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - 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