Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)C1OC(C(O)C1O)N1C=NC2=C1N=C(N=C2N)C#CC1=CC=C(F)C=C1

InChIKey

InChIKey=IVQJCRPENRVNSX-UHFFFAOYSA-N

Formula

C20H19FN6O4

Mass

426.408

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Halobenzene - Fluorobenzene - N-substituted imidazole - Aryl fluoride - Aryl halide - Pyrimidine - Benzenoid - Imidolactam - Monocyclic benzene moiety - Oxolane - Imidazole - Heteroaromatic compound - Azole - 1,2-diol - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organohalogen compound - Alcohol - Carbonyl group - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organofluoride - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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