Compound Identification
SMILES
CC(C)OP(=O)(COCCOC1=NC(N)=NC(N)=C1)OC(C)C
InChIKey
InChIKey=PXPFACYWCXSPRV-UHFFFAOYSA-N
Formula
C13H25N4O5P
Mass
348.34
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Acyclic 2,4-diaminopyrimidine nucleoside phosphonates
Intermediate Tree Nodes
Not available
Direct Parent
Acyclic 2,4-diaminopyrimidine nucleoside phosphonates
Alternative Parents
Dialkyl alkylphosphonates Aminopyrimidines and derivatives Alkyl aryl ethers Phosphonic acid esters Imidolactams Heteroaromatic compounds Azacyclic compounds Primary amines Organophosphorus compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
2,4-diaminopyrimidine nucleoside phosphonate - Alkyl aryl ether - Aminopyrimidine - Dialkyl alkylphosphonate - Phosphonic acid diester - Phosphonic acid ester - Pyrimidine - Imidolactam - Organophosphonic acid derivative - Heteroaromatic compound - Ether - Azacycle - Organoheterocyclic compound - Amine - Hydrocarbon derivative - Primary amine - Organic oxide - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as acyclic 2,4-diaminopyrimidine nucleoside phosphonates. These are pyrimidine nucleoside analogues with a structure that is characterized by a phosphonylmethoxyethoxyl group that is linked to the N1 atom of a 2,4-diaminopyrimidine.
External Descriptors
Not available