Compound Identification
SMILES
CC(C)OP(=O)(COCCOC1=NC(N)=NC(N)=C1Cl)OC(C)C
InChIKey
InChIKey=DMFPUXMVYRPTGQ-UHFFFAOYSA-N
Formula
C13H24ClN4O5P
Mass
382.78
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
Halopyrimidines Dialkyl alkylphosphonates Aminopyrimidines and derivatives Alkyl aryl ethers Phosphonic acid esters Imidolactams Aryl chlorides Heteroaromatic compounds Azacyclic compounds Primary amines Organophosphorus compounds Organochlorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
2,4-diaminopyrimidine nucleoside phosphonate - Alkyl aryl ether - Aminopyrimidine - Dialkyl alkylphosphonate - Halopyrimidine - Phosphonic acid diester - Aryl chloride - Aryl halide - Phosphonic acid ester - Pyrimidine - Imidolactam - Heteroaromatic compound - Organophosphonic acid derivative - Azacycle - Organoheterocyclic compound - Ether - Primary amine - Organonitrogen compound - Organochloride - Organooxygen compound - Organohalogen compound - Organic oxide - Organophosphorus compound - Amine - Hydrocarbon derivative - 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