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Structure Information
Structure

Compound Identification

SMILES

CC(=O)NC1=NC(=O)N(C=C1)C1CSC(CO)O1

InChIKey

InChIKey=NKMKJZRNUUXFOB-UHFFFAOYSA-N

Formula

C10H13N3O4S

Mass

271.29

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

3'-thia pyrimidine nucleosides

Intermediate Tree Nodes

Not available

Direct Parent

3'-thia pyrimidine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

3'-thia pyrimidine nucleoside - N-acetylarylamine - N-arylamide - Pyrimidone - Hydropyrimidine - Pyrimidine - Imidolactam - Monothioacetal - Oxathiolane - Heteroaromatic compound - Acetamide - Carboxamide group - Secondary carboxylic acid amide - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Primary alcohol - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Alcohol - Carbonyl group - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as 3'-thia pyrimidine nucleosides. These are nucleoside analogues with a structure that consists of a pyrimidine base, which is N-substituted at the 1-position with a 3'-thia derivative (1,3-oxazolidine) of the ribose moiety that is characteristic of nucleosides.

External Descriptors

Not available

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