You are using an unsupported browser. Please upgrade your browser to a newer version to get the best experience on ClassyFire.
Structure Information
Structure

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

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

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

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

Previous Back Next