Compound Identification
SMILES
CC(C)OC(=O)OCOP(=O)(COC(C)CN1C=NC2=C1C=CC=C2N)OCOC(=O)OC(C)C
InChIKey
InChIKey=UBKAMVQIWGOZDM-UHFFFAOYSA-N
Formula
C21H32N3O10P
Mass
517.472
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Acyclic purine nucleoside phosphonates
Intermediate Tree Nodes
Not available
Direct Parent
Acyclic purine nucleoside phosphonates
Alternative Parents
Benzimidazoles Dialkyl alkylphosphonates Phosphonic acid esters N-substituted imidazoles Carbonic acid diesters Benzenoids Heteroaromatic compounds Azacyclic compounds Primary amines Organophosphorus compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Acyclic purine nucleoside phosphonate - Benzimidazole - Dialkyl alkylphosphonate - Phosphonic acid diester - Carbonic acid diester - N-substituted imidazole - Phosphonic acid ester - Benzenoid - Azole - Imidazole - Organophosphonic acid derivative - Heteroaromatic compound - Carbonic acid derivative - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Amine - Organic oxide - Carbonyl group - Organic oxygen compound - Primary amine - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as acyclic purine nucleoside phosphonates. These are purine nucleoside analogues with a structure that is characterized by a phosphonylmethoxyethoxyl group that is linked to the N1 atom of a purine.
External Descriptors
Not available