Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@@H](CCl)O[C@H]([C@@H]1O)N1C=NC2=C1N=C(Cl)N=C2NN1CCC(CC1)SC1=CC=CC=C1

InChIKey

InChIKey=ZWMXNEWPLAOIAZ-WVSUBDOOSA-N

Formula

C21H24Cl2N6O3S

Mass

511.42

Export to:

JSON SDF CSV

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 - Pentose monosaccharide - Imidazopyrimidine - Purine - Aryl thioether - Thiophenol ether - 2-halopyrimidine - Halopyrimidine - Alkylarylthioether - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Piperidine - Pyrimidine - Benzenoid - Imidolactam - Heteroaromatic compound - Oxolane - Azole - Imidazole - 1,2-diol - Secondary alcohol - Organoheterocyclic compound - Sulfenyl compound - Azacycle - Thioether - Oxacycle - Alkylhydrazine - Alkyl chloride - Hydrazine derivative - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Alcohol - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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

Previous Back Next