Compound Identification
SMILES
CC(C)(C)O[P+](=O)OC[C@@H]1CC[C@@H](O1)N1C=NC2=C1NC(N)=NC2=O
InChIKey
InChIKey=YXWQSWACXMBAJK-DTWKUNHWSA-O
Formula
C14H21N5O5P
Mass
370.325
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 6-oxopurines Hypoxanthines Pyrimidones Aminopyrimidines and derivatives N-substituted imidazoles Vinylogous amides Oxolanes Heteroaromatic compounds Oxacyclic compounds Azacyclic compounds Primary amines Hydrocarbon derivatives Organic oxides Organooxygen compounds Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine ribonucleoside phosphonate - Purine 2',3'-dideoxyribonucleoside - Purine nucleoside - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Oxolane - Vinylogous amide - Organoheterocyclic compound - Azacycle - Oxacycle - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Organic oxide - 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