Structure Information
Structure

Compound Identification

SMILES

COC1=NC(Cl)=NC2=C1N=CN2C1O[C@H](CO)[C@@H](O)[C@@H]1F

InChIKey

InChIKey=UCJFUCMRTLLOEN-FRSABSTQSA-N

Formula

C11H12ClFN4O4

Mass

318.69

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 2'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 2'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside - Hypoxanthine - Imidazopyrimidine - Purine - Alkyl aryl ether - 2-halopyrimidine - Halopyrimidine - Aryl chloride - Aryl halide - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Oxolane - Fluorohydrin - Halohydrin - Secondary alcohol - Oxacycle - Ether - Azacycle - Organoheterocyclic compound - Organooxygen compound - Primary alcohol - Alkyl halide - Alkyl fluoride - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organofluoride - Organochloride - Organohalogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.

External Descriptors

Not available

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