Compound Identification
SMILES
CCCCCCCCCCCCCCCCCCOC[C@@H](COP(O)(=O)CO[C@H](CO)CN1C=NC2=C1C=CC=C2N)OCC1=CC=CC=C1
InChIKey
InChIKey=PENSKGMRHKSZGK-ZPGRZCPFSA-N
Formula
C39H64N3O7P
Mass
717.929
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
Glycerophosphonolipids Benzylethers Benzimidazoles Glycerol ethers Phosphonic acid esters N-substituted imidazoles Organic phosphonic acids Heteroaromatic compounds Dialkyl ethers Azacyclic compounds Primary amines Primary alcohols Organophosphorus compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Acyclic purine nucleoside phosphonate - Glycerophosphonolipid - Benzimidazole - Benzylether - Glycerol ether - Monocyclic benzene moiety - N-substituted imidazole - Benzenoid - Phosphonic acid ester - Azole - Heteroaromatic compound - Imidazole - Organophosphonic acid - Organophosphonic acid derivative - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Primary amine - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - Organonitrogen compound - Organooxygen compound - Organophosphorus 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