Structure Information
Structure

Compound Identification

SMILES

CC1(OP(O)(=O)OP(O)(=O)OOC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(=O)NC2=O)O[C@H](CO)[C@H](O)[C@H](S)[C@H]1S

InChIKey

InChIKey=QJKLSMFPXIEGIG-AHBWNYEJSA-N

Formula

C16H26N2O16P2S2

Mass

628.45

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Organic pyrophosphate - Monoalkyl phosphate - Pyrimidone - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Oxane - Phosphoric acid ester - Alkyl phosphate - Pyrimidine - Heteroaromatic compound - Oxolane - Vinylogous amide - Secondary alcohol - Urea - Lactam - Alkylthiol - Organoheterocyclic compound - Oxacycle - Azacycle - Organosulfur compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Primary alcohol - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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