Structure Information
Structure

Compound Identification

SMILES

NC1=NC(N)=C(Cl)C(OCCOCP(O)(O)=O)=N1

InChIKey

InChIKey=QBUGISJBWNVBKD-UHFFFAOYSA-N

Formula

C7H12ClN4O5P

Mass

298.62

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Taxonomic Classification

Taxonomy Tree

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

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

2,4-diaminopyrimidine nucleoside phosphonate - Alkyl aryl ether - Aminopyrimidine - Halopyrimidine - Aryl chloride - Aryl halide - Imidolactam - Pyrimidine - Heteroaromatic compound - Organophosphonic acid - Organophosphonic acid derivative - Ether - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organochloride - Organic oxygen compound - Amine - Organohalogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Organooxygen compound - Organophosphorus compound - Primary amine - 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

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