Structure Information
Structure

Compound Identification

SMILES

CCC(=O)N1CCC(CC1)NC1=NC(Cl)=NC2=C1N=CN2[C@@H]1O[C@H](CF)[C@@H](O)[C@H]1O

InChIKey

InChIKey=KDPAKFYACHSDPF-IWCJZZDYSA-N

Formula

C18H24ClFN6O4

Mass

442.88

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-deoxyribonucleoside - N-glycosyl compound - Glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - N-acyl-piperidine - Purine - Halopyrimidine - 2-halopyrimidine - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Imidolactam - Aryl halide - Aryl chloride - Piperidine - Pyrimidine - Azole - Oxolane - Heteroaromatic compound - Imidazole - Tertiary carboxylic acid amide - 1,2-diol - Carboxamide group - Secondary alcohol - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Oxacycle - Organic nitrogen compound - Organohalogen compound - Organochloride - Organofluoride - Carbonyl group - Organonitrogen compound - Organooxygen compound - 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 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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