Structure Information
Structure

Compound Identification

SMILES

CNC(=O)[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)n1cnc2c(N[C@@H]3C[C@H]3c3ccc(F)c(F)c3)nc(nc12)C#Cc1ccccn1

InChIKey

InChIKey=LGMZGZAJMOELBF-BAJVYAFTSA-N

Formula

C29H25F2N7O3

Mass

557.562

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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 - Imidazopyrimidine - Purine - Fluorobenzene - Halobenzene - Aminopyrimidine - Secondary aliphatic/aromatic amine - Cyclopropanecarboxylic acid or derivatives - Aryl fluoride - N-substituted imidazole - Monocyclic benzene moiety - Aryl halide - Pyridine - Pyrimidine - Benzenoid - Imidolactam - Heteroaromatic compound - Azole - Imidazole - Cyclic alcohol - Amino acid or derivatives - 1,2-diol - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Azacycle - Secondary amine - Organoheterocyclic compound - Carboxylic acid derivative - Organic nitrogen compound - Organohalogen compound - Carbonyl group - Organofluoride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Amine - Alcohol - Organic oxygen 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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