Structure Information
Structure

Compound Identification

SMILES

Nc1ccn(C2CC(O)C(C2)OCP(O)(O)=O)c(=O)n1

InChIKey

InChIKey=LREXMUIAVQJGOC-UHFFFAOYSA-N

Formula

C10H16N3O6P

Mass

305.227

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Phosphonated cyclopentyl nucleosides

Intermediate Tree Nodes

1,3-substituted phosphonated cyclopentyl nucleosides

Direct Parent

1,3-substituted phosphonated cyclopentyl pyrimidine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

1,3-substituted phosphonated cyclopentyl pyrimidine nucleoside - Cyclopentyl nucleoside - Pyrimidone - Aminopyrimidine - Imidolactam - Pyrimidine - Hydropyrimidine - Cyclopentanol - Heteroaromatic compound - Organophosphonic acid derivative - Organophosphonic acid - Cyclic alcohol - Secondary alcohol - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as 1,3-substituted phosphonated cyclopentyl pyrimidine nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a phosphonate group, and at the 3-position with either a pyrimidine base.

External Descriptors

Not available

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