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Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1C[C@H](N=[N+]=[N-])[C@@H](S1)N1C=NC2=C1N=CN=C2Cl

InChIKey

InChIKey=NWBOSDXEMSFRBL-GOZTUDAPSA-N

Formula

C10H10ClN7OS

Mass

311.75

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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 - Imidazopyrimidine - Purine - Halopyrimidine - Aryl chloride - Aryl halide - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Thiolane - Azo compound - Azo imide - Azacycle - Organoheterocyclic compound - Dialkylthioether - Thioether - Organohalogen compound - Organic oxygen compound - Organic zwitterion - Organic nitrogen compound - Organic salt - Alcohol - Hydrocarbon derivative - Organochloride - Organonitrogen compound - Organooxygen compound - Primary alcohol - 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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