Structure Information
Structure

Compound Identification

SMILES

NC1=NC(Cl)=NC2=C1N=CN2[C@@H]1S[C@H](COCC2=CC=CC=C2)[C@@H](OCC2=CC=CC=C2)[C@@H]1OCC1=CC=CC=C1

InChIKey

InChIKey=FWYVESCERKITLL-JVYBIVSJSA-N

Formula

C31H30ClN5O3S

Mass

588.12

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Thionucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Thionucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine thionucleoside - 6-aminopurine - Benzylether - Imidazopyrimidine - Purine - 2-halopyrimidine - Aminopyrimidine - Halopyrimidine - Imidolactam - Aryl chloride - Aryl halide - Benzenoid - Pyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Heteroaromatic compound - Thiolane - Azole - Imidazole - Azacycle - Organoheterocyclic compound - Dialkylthioether - Thioether - Dialkyl ether - Ether - Hydrocarbon derivative - Organic nitrogen compound - Primary amine - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Amine - Organochloride - Organohalogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as thionucleosides. These are nucleoside analogues that contain a thiolane or a thietane that is 1,3-disubstituted with a hydroxyl group and pyrimidine or purine base, at the 1- and 3-position, respectively.

External Descriptors

Not available

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