Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)C(O)=O)O2)C(=O)NC1=O

InChIKey

InChIKey=WNUWWHMCMPDGLG-LHBOOPKSSA-N

Formula

C16H24N2O17P2

Mass

578.313

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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 2'-deoxyribonucleoside diphosphate - Pentose phosphate - Glucuronic acid or derivatives - Organic pyrophosphate - Monosaccharide phosphate - Beta-hydroxy acid - Pyrimidone - Monoalkyl phosphate - Oxane - Hydropyrimidine - Phosphoric acid ester - Hydroxy acid - Pyran - Pyrimidine - Organic phosphoric acid derivative - Alkyl phosphate - Monosaccharide - Tetrahydrofuran - Heteroaromatic compound - Vinylogous amide - Secondary alcohol - Urea - Lactam - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Carbonyl group - Alcohol - Organic oxygen compound - Organonitrogen compound - Organooxygen 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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