Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(=O)NC2=O)[C@H](F)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=NGTCPFGWXMBZEP-NQQHDEILSA-N

Formula

C15H23FN2O16P2

Mass

568.293

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Subclass

Pyrimidine nucleotide sugars

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine nucleotide sugars

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine nucleotide sugar - Pyrimidine ribonucleoside diphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Organic pyrophosphate - Pyrimidone - Monoalkyl phosphate - Alkyl phosphate - Pyrimidine - Hydropyrimidine - Phosphoric acid ester - Monosaccharide - Oxane - Organic phosphoric acid derivative - Vinylogous amide - Tetrahydrofuran - Heteroaromatic compound - Urea - Secondary alcohol - Fluorohydrin - Halohydrin - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Organooxygen compound - Organohalogen compound - Hydrocarbon derivative - Organopnictogen compound - Primary alcohol - Alkyl halide - Alkyl fluoride - Organic oxygen compound - Organic nitrogen compound - Alcohol - Organic oxide - Organofluoride - Organonitrogen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group.

External Descriptors

Not available

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