Compound Identification
SMILES
CC1(C)O[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O1)N1C(Br)=NC2=C1N=CN=C2N
InChIKey
InChIKey=GDKUQUVKGLVGBN-IOSLPCCCSA-N
Formula
C13H16BrN5O4
Mass
386.206
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-aminopurines Aminopyrimidines and derivatives Ketals Primary aromatic amines Aryl bromides N-substituted imidazoles Monosaccharides Imidolactams 1,3-dioxolanes Oxolanes Heteroaromatic compounds Oxacyclic compounds Azacyclic compounds Organobromides Organopnictogen compounds Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Ketal - Aryl bromide - Aryl halide - Monosaccharide - N-substituted imidazole - Primary aromatic amine - Pyrimidine - Imidolactam - Oxolane - Heteroaromatic compound - Meta-dioxolane - Azole - Imidazole - Oxacycle - Azacycle - Organoheterocyclic compound - Acetal - Amine - Alcohol - Organopnictogen compound - Organohalogen compound - Organobromide - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organic oxygen compound - Primary alcohol - Primary amine - 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