Compound Identification
SMILES
CC(C)OP(=O)(COCCN1C=NC2=C1C=CC=C2N)OC(C)C
InChIKey
InChIKey=KCHRMVQEJIYWNO-UHFFFAOYSA-N
Formula
C16H26N3O4P
Mass
355.375
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 Benzenoids Heteroaromatic compounds Azacyclic compounds Primary amines Organophosphorus compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Acyclic purine nucleoside phosphonate - Benzimidazole - Dialkyl alkylphosphonate - Phosphonic acid diester - N-substituted imidazole - Phosphonic acid ester - Benzenoid - Azole - Imidazole - Heteroaromatic compound - Organophosphonic acid derivative - Azacycle - Organoheterocyclic compound - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Primary amine - 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