Compound Identification
SMILES
OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N1CCN(CC1)C(C1=CC=CC=C1)C1=CC=CC=C1
InChIKey
InChIKey=UZTOPZJPIWBRSJ-ZCIWVVNKSA-N
Formula
C27H30N6O4
Mass
502.575
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
Diphenylmethanes N-arylpiperazines 6-alkylaminopurines Glycosylamines Pentoses Dialkylarylamines Aminopyrimidines and derivatives Aralkylamines N-alkylpiperazines N-substituted imidazoles Imidolactams Heteroaromatic compounds Oxolanes 1,2-diols Secondary alcohols Trialkylamines Oxacyclic compounds Azacyclic compounds Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Diphenylmethane - N-arylpiperazine - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Dialkylarylamine - Aminopyrimidine - Aralkylamine - N-alkylpiperazine - Monocyclic benzene moiety - 1,4-diazinane - Monosaccharide - N-substituted imidazole - Piperazine - Imidolactam - Benzenoid - Pyrimidine - Oxolane - Imidazole - Heteroaromatic compound - Azole - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Primary alcohol - Hydrocarbon derivative - Alcohol - Amine - 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