Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)[C@@H]1CCC[C@H]1OCP(O)(O)=O

InChIKey

InChIKey=UXGWVPXRBHYJFV-HTQZYQBOSA-N

Formula

C10H16N3O5P

Mass

289.228

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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

1,2-substituted phosphonated cyclopentyl nucleosides

Direct Parent

1,2-substituted phosphonated cyclopentyl pyrimidine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

1,2-substituted phosphonated cyclopentyl pyrimidine nucleoside - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Pyrimidine - Imidolactam - Organophosphonic acid - Organophosphonic acid derivative - Heteroaromatic compound - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Primary amine - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Amine - Organic oxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as 1,2-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 2-position with either a pyrimidine base.

External Descriptors

Not available

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