Compound Identification
SMILES
NC1=NC=NC2=C1N=CN2[C@H]1CC[C@@H](CO[P+](=O)OC23CCC(CC2)C3)O1
InChIKey
InChIKey=LDDPGFCSTIMTHP-XPFWZQFZSA-N
Formula
C17H23N5O4P
Mass
392.375
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',3'-dideoxyribonucleosides Aromatic monoterpenoids 6-aminopurines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Oxacyclic compounds Azacyclic compounds Primary amines Organooxygen compounds Organic oxides Hydrocarbon derivatives Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine ribonucleoside phosphonate - Purine 2',3'-dideoxyribonucleoside - Purine nucleoside - 6-aminopurine - Aromatic monoterpenoid - Monoterpenoid - Norbornane monoterpenoid - Imidazopyrimidine - Purine - Aminopyrimidine - Imidolactam - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Oxolane - Heteroaromatic compound - Organoheterocyclic compound - Azacycle - Oxacycle - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Primary amine - Hydrocarbon derivative - Amine - 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