Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1S[C@@H](C[C@@H]1N=[N+]=[N-])N1C=C(Cl)C(=O)NC1=O

InChIKey

InChIKey=FYDAAGUWNIHUEX-XVMARJQXSA-N

Formula

C9H10ClN5O3S

Mass

303.72

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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 heteromonocyclic compounds

Substituents

Pyrimidine thionucleoside - Halopyrimidine - Pyrimidone - Aryl chloride - Aryl halide - Hydropyrimidine - Pyrimidine - Vinylogous amide - Heteroaromatic compound - Thiolane - Urea - Azo compound - Azo imide - Lactam - Dialkylthioether - Azacycle - Organoheterocyclic compound - Thioether - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Primary alcohol - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organic zwitterion - Organic oxide - Organic salt - Aromatic heteromonocyclic 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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