Structure Information
Structure

Compound Identification

SMILES

OC[C@@H]1C[C@H](N=[N+]=[N-])[C@H](S1)N1C=NC2=C1NC=NC2=O

InChIKey

InChIKey=LYIMYZMUCXHUKQ-VGIXGZPDSA-N

Formula

C10H11N7O2S

Mass

293.31

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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-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Pyrimidone - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Thiolane - Azo compound - Azo imide - Organoheterocyclic compound - Azacycle - Dialkylthioether - Thioether - Organic salt - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Primary alcohol - Organic zwitterion - 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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