Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@@H](CF)O[C@H]([C@@H]1O)N1C=NC2=C1N=C(Cl)N=C2NC1CCOCC1

InChIKey

InChIKey=DETMIFBOBYBZCW-IDTAVKCVSA-N

Formula

C15H19ClFN5O4

Mass

387.8

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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 - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - Imidolactam - Aryl halide - Pyrimidine - Aryl chloride - Monosaccharide - Oxane - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Oxolane - 1,2-diol - Secondary alcohol - Dialkyl ether - Ether - Organoheterocyclic compound - Azacycle - Oxacycle - Organonitrogen compound - Alcohol - Alkyl fluoride - Organic nitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Amine - Alkyl halide - Organohalogen compound - Organochloride - Organofluoride - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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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