Compound Identification
SMILES
ONC1=NC(=O)N(C=C1F)[C@H]1C[C@H](O)[C@@H](CO[P+](O)=O)O1
InChIKey
InChIKey=JXIUCJDQFFYDOC-RRKCRQDMSA-P
Formula
C9H12FN3O7P
Mass
324.181
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Deoxyribo- and ribonucleoside phosphonates
Subclass
Purine ribonucleoside phosphonates
Intermediate Tree Nodes
Not available
Direct Parent
Purine ribonucleoside phosphonates
Alternative Parents
Pyrimidine 2'-deoxyribonucleosides Arylhydroxamates Pyrimidones Halopyrimidines Aryl fluorides Hydropyrimidines Imidolactams Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds N-organohydroxylamines Organic oxides Hydrocarbon derivatives Organofluorides Organic cations
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Purine ribonucleoside phosphonate - Pyrimidine 2'-deoxyribonucleoside - Pyrimidine nucleoside - Arylhydroxamate - Halopyrimidine - Pyrimidone - Aryl fluoride - Aryl halide - Hydropyrimidine - Pyrimidine - Imidolactam - Heteroaromatic compound - Oxolane - Secondary alcohol - Oxacycle - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Alcohol - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organic cation - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as purine ribonucleoside phosphonates. These are n-glycosyl compound that possess both a purine nucleobase linked to either a ribose or deoxyribose, which in turn carries a phosphonate group at the 5'-position.
External Descriptors
Not available