Compound Identification
SMILES
CC1=CN([C@H]2C[C@H](F)[C@@H](CO[P+](=O)OC34CCC(CC3)C4)O2)C(=O)NC1=O
InChIKey
InChIKey=GIHAKOPKLDWKSU-GBDWWVHMSA-O
Formula
C17H23FN2O6P
Mass
401.351
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',3'-dideoxyribonucleosides Aromatic monoterpenoids Bicyclic monoterpenoids Pyrimidones Hydropyrimidines Vinylogous amides Oxolanes Heteroaromatic compounds Ureas Lactams Oxacyclic compounds Azacyclic compounds Organofluorides Hydrocarbon derivatives Organonitrogen compounds Organooxygen compounds Alkyl fluorides Organic oxides Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine ribonucleoside phosphonate - Pyrimidine 2',3'-dideoxyribonucleoside - Pyrimidine nucleoside - Aromatic monoterpenoid - Bicyclic monoterpenoid - Monoterpenoid - Norbornane monoterpenoid - Pyrimidone - Hydropyrimidine - Pyrimidine - Vinylogous amide - Heteroaromatic compound - Oxolane - Urea - Lactam - Azacycle - Oxacycle - Organoheterocyclic compound - Alkyl halide - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organic oxide - Hydrocarbon derivative - Alkyl fluoride - Organic oxygen compound - Organic cation - Aromatic heteropolycyclic 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