Compound Identification
SMILES
OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(\C=C/F)N=C2Cl
InChIKey
InChIKey=GQVAWTIAPBZGMU-FIEZPMIPSA-N
Formula
C12H12ClFN4O4
Mass
330.7
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
Glycosylamines Pentoses Purines and purine derivatives Halopyrimidines N-substituted imidazoles Aryl chlorides Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Vinyl fluorides Fluoroalkenes Azacyclic compounds Organonitrogen compounds Organofluorides Organochlorides Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Imidazopyrimidine - Purine - Halopyrimidine - Aryl chloride - Aryl halide - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - Organoheterocyclic compound - Vinyl fluoride - Vinyl halide - Oxacycle - Azacycle - Fluoroalkene - Haloalkene - Organic oxygen compound - Organohalogen compound - Organochloride - Organic nitrogen compound - Organofluoride - Hydrocarbon derivative - Alcohol - Primary alcohol - Organonitrogen compound - Organooxygen 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