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Structure Information
Structure

Compound Identification

SMILES

CCOP(=O)(COC1CC(C=C1)N1C=CC(N=CN(C)C)=NC1=O)OCC

InChIKey

InChIKey=IMSUGPHBXNDJFS-UHFFFAOYSA-N

Formula

C17H27N4O5P

Mass

398.4

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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 - Dialkyl alkylphosphonate - Pyrimidone - Phosphonic acid diester - Hydropyrimidine - Phosphonic acid ester - Pyrimidine - Organophosphonic acid derivative - Heteroaromatic compound - Tertiary amine - Amidine - Carboxylic acid amidine - Formamidine - Azacycle - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Organophosphorus compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Amine - Organic nitrogen compound - Organonitrogen compound - 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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