Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)[C@@H]1CS[C@H](CO)O1.CC(=O)SCCOP(=O)(OCCOCN1C=NC2=C1NC(N)=NC2=O)OCCSC(C)=O

InChIKey

InChIKey=XPRZUJCLNNXLPE-HLISZSCWSA-N

Formula

C24H35N8O11PS3

Mass

738.74

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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 - 6-oxopurine - Purinone - Hypoxanthine - Purine - Imidazopyrimidine - Trialkyl phosphate - Pyrimidone - Aminopyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Primary aromatic amine - Imidolactam - Hydropyrimidine - Alkyl phosphate - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Monothioacetal - Heteroaromatic compound - Oxathiolane - Vinylogous amide - Thiocarboxylic acid ester - Carbothioic s-ester - Amino acid or derivatives - Thiocarboxylic acid or derivatives - Azacycle - Sulfenyl compound - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Primary amine - Amine - Hydrocarbon derivative - Alcohol - Organic oxide - Organopnictogen compound - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Primary alcohol - Aromatic heteropolycyclic 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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