Compound Identification
SMILES
OCC1OC(F)(C(O)C1O)N1C=CC(=O)NC1=O.CC1=CN(C2CCC(CO[P+](O)=O)O2)C(=O)NC1=O
InChIKey
InChIKey=DODQUPDESWOMNK-UHFFFAOYSA-P
Formula
C19H25FN4O12P
Mass
551.397
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 Pyrimidones Hydropyrimidines Monosaccharides Vinylogous amides Oxolanes Heteroaromatic compounds Lactams Fluorohydrins Ureas Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary alcohols Organonitrogen compounds Organofluorides Organic oxides Alkyl fluorides Hydrocarbon derivatives Organic cations
Molecular Framework
Not available
Substituents
Purine ribonucleoside phosphonate - Pyrimidine 2',3'-dideoxyribonucleoside - Pyrimidine nucleoside - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Vinylogous amide - Heteroaromatic compound - Oxolane - Urea - Secondary alcohol - Fluorohydrin - Halohydrin - Lactam - Azacycle - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Alkyl fluoride - Organic nitrogen compound - Alcohol - Organic oxygen compound - Alkyl halide - 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