Compound Identification
SMILES
CC1(C)OCC(CNC2=NC=NC3=C2N=CN3[C@@H]2O[C@H](CO)[C@@H](O)[C@@]2(C)O)O1
InChIKey
InChIKey=HFVXXEOTQJBJGS-UWXSQHSLSA-N
Formula
C17H25N5O6
Mass
395.416
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 Secondary alkylarylamines Aminopyrimidines and derivatives Ketals Imidolactams Monosaccharides N-substituted imidazoles Tertiary alcohols Oxolanes 1,3-dioxolanes Heteroaromatic compounds Secondary alcohols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Ketal - Aminopyrimidine - Secondary aliphatic/aromatic amine - Monosaccharide - Imidolactam - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - Meta-dioxolane - Imidazole - Oxolane - Tertiary alcohol - Secondary alcohol - Acetal - Organoheterocyclic compound - Azacycle - Oxacycle - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organooxygen compound - Organic oxygen compound - Primary alcohol - Organic nitrogen 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