Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)[C@H]1O[C@H]([C@@H](O)C1O)N1C=NC2=C1N=C(N=C2N)C#CCC1CCN(CC1)C(=O)OC1=CC(F)=C(F)C=C1

InChIKey

InChIKey=RUDDTMBVDJIDKZ-QMXBHJOJSA-N

Formula

C27H29F2N7O6

Mass

585.569

Export to:

JSON SDF CSV

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

Previous Back Next