Compound Identification
SMILES
CC(C)O[C@@H]1[C@@H](CO[P+](O)=O)O[C@H]([C@@H]1OC(C)C)[N+]1=CN(C)C2=C1NC(N)=NC2=O
InChIKey
InChIKey=DYMXGGQOJYPGFV-XNIJJKJLSA-P
Formula
C17H28N5O7P
Mass
445.412
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 nucleosides Glycosylamines 6-oxopurines Hypoxanthines Pyrimidones Aminopyrimidines and derivatives Monosaccharides N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Oxolanes Oxacyclic compounds Dialkyl ethers Azacyclic compounds Primary amines Hydrocarbon derivatives Organic oxides Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine ribonucleoside phosphonate - Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Oxolane - Vinylogous amide - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Dialkyl ether - Organonitrogen compound - Organic oxygen compound - Amine - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Primary amine - Organic nitrogen 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