Compound Identification
SMILES
CCCOC1=CC2=C(C=C1)C(CC2)NC1=NC=NC2=C1N=CN2C1OC(CO)C(O)C1O
InChIKey
InChIKey=UWTTXYWKHZQTKW-UHFFFAOYSA-N
Formula
C22H27N5O5
Mass
441.488
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 Indanes Phenol ethers Alkyl aryl ethers Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Amines Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - Pentose monosaccharide - 6-aminopurine - Indane - Imidazopyrimidine - Purine - Phenol ether - Aminopyrimidine - Alkyl aryl ether - Monosaccharide - N-substituted imidazole - Imidolactam - Benzenoid - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Oxolane - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Organic nitrogen compound - Amine - Organic oxygen compound - Hydrocarbon derivative - Alcohol - 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