Structure Information
Structure

Compound Identification

SMILES

NC1=NC(N\N=N\C(=O)NC2=CC=CC(=C2)C(F)(F)F)=NC2=C1N=CN2C1O[C@H](CO)[C@@H](O)[C@H]1O

InChIKey

InChIKey=NIJHCHQAXCSLGV-FJFSNTMWSA-N

Formula

C18H18F3N9O5

Mass

497.395

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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 - Glycosyl compound - N-glycosyl compound - N-phenylurea - 6-aminopurine - Trifluoromethylbenzene - Pentose monosaccharide - Purine - Imidazopyrimidine - Aminopyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Monosaccharide - Pyrimidine - Imidolactam - Benzenoid - Oxolane - Azole - Heteroaromatic compound - Imidazole - 1,2-diol - Secondary alcohol - Organic 1,3-dipolar compound - Organoheterocyclic compound - Azacycle - Propargyl-type 1,3-dipolar organic compound - Oxacycle - Organic nitrogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Primary alcohol - Carbonyl group - Primary amine - Hydrocarbon derivative - Organic oxide - Amine - Alkyl halide - Alkyl fluoride - Alcohol - Organic oxygen compound - 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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