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Structure Information
Structure

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

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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 - 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

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