Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](C(F)SC2=CC=C(Cl)C=C2)[C@@H](O)[C@H]1O

InChIKey

InChIKey=NNYXXBJNHHWVBK-HRZZRIEESA-N

Formula

C16H15ClFN5O3S

Mass

411.84

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

5'-deoxy-5'-thionucleosides

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxy-5'-thionucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-deoxy-5'-thionucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aryl thioether - Thiophenol ether - Aminopyrimidine - Chlorobenzene - Halobenzene - Alkylarylthioether - Aryl chloride - Aryl halide - Monocyclic benzene moiety - N-substituted imidazole - Imidolactam - Pyrimidine - Benzenoid - Oxolane - Azole - Heteroaromatic compound - Imidazole - Secondary alcohol - 1,2-diol - Sulfenyl compound - Thioether - Oxacycle - Organoheterocyclic compound - Azacycle - Organosulfur compound - Alkyl fluoride - Organohalogen compound - Hydrocarbon derivative - Alcohol - Organochloride - Organic nitrogen compound - Organofluoride - Primary amine - Alkyl halide - Amine - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxy-5'-thionucleosides. These are 5'-deoxyribonucleosides in which the ribose is thio-substituted at the 5'position by a S-alkyl group.

External Descriptors

Not available

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