Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1C[C@H](C=C1)N1C=NC2=C1N=C(NC1=C3C=C(F)C=CC3=NC1=O)N=C2NC1CC1

InChIKey

InChIKey=WFOCJQHTDPNHHP-RISCZKNCSA-N

Formula

C22H20FN7O2

Mass

433.447

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Cyclopentyl nucleosides

Intermediate Tree Nodes

1,3-substituted cyclopentyl nucleosides

Direct Parent

1,3-substituted cyclopentyl purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1,3-substituted cyclopentyl purine nucleoside - 6-alkylaminopurine - 6-aminopurine - Alpha-amino acid or derivatives - Imidazopyrimidine - Indole or derivatives - Purine - Aminopyrimidine - Aryl fluoride - Aryl halide - Imidolactam - Benzenoid - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - N-acylimine - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Primary alcohol - Organohalogen compound - Organic oxygen compound - Organofluoride - Carbonyl group - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

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

External Descriptors

Not available

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