Compound Identification
SMILES
CNC1=NC=NC2=C1N=CN2[C@H]1C[C@H](O)[C@@H](CO[P+](=O)OP(O)(=O)O[P+](O)=O)O1
InChIKey
InChIKey=SPKQTCGMOUFFPJ-XLPZGREQSA-P
Formula
C11H16N5O10P3
Mass
471.194
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
Purine 2'-deoxyribonucleosides 6-alkylaminopurines Secondary alkylarylamines Aminopyrimidines and derivatives Organic phosphoric acids and derivatives N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine ribonucleoside phosphonate - Purine 2'-deoxyribonucleoside - Purine nucleoside - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - N-substituted imidazole - Organic phosphoric acid derivative - Pyrimidine - Imidolactam - Heteroaromatic compound - Oxolane - Azole - Imidazole - Secondary alcohol - Azacycle - Organoheterocyclic compound - Oxacycle - Secondary amine - Organic oxygen compound - Amine - Alcohol - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - 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