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Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)[C@@H]1CS[C@H](CO)O1.OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)C1C=CC(=O)NC1=O

InChIKey

InChIKey=KWGKMKMJDJFJCS-BCHHXAQYSA-N

Formula

C18H24N4O9S

Mass

472.47

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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

Not available

Substituents

3'-thia pyrimidine nucleoside - C-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Aminopyrimidine - Pyrimidone - Monosaccharide - Hydropyrimidine - Pyrimidine - Imidolactam - Hydropyridine - Carboxylic acid imide - Oxathiolane - Monothioacetal - Carboxylic acid imide, n-unsubstituted - Heteroaromatic compound - Oxolane - Dicarboximide - Secondary alcohol - 1,2-diol - Carboxylic acid derivative - Dialkyl ether - Oxacycle - Ether - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Amine - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - 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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