Structure Information
Structure

Compound Identification

SMILES

CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.OC[C@H]1OC(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](O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=WXPMDPMEMUHXNQ-FAVRMQPISA-L

Formula

C47H94N4O17P2

Mass

1049.228

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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

Not available

Substituents

Pyrimidine nucleotide sugar - Pyrimidine ribonucleoside diphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Organic pyrophosphate - Pyrimidone - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Oxane - Phosphoric acid ester - Alkyl phosphate - Pyrimidine - Tetraalkylammonium salt - Heteroaromatic compound - Oxolane - Vinylogous amide - Quaternary ammonium salt - Secondary alcohol - Urea - Lactam - 1,2-diol - Organoheterocyclic compound - Polyol - Azacycle - Oxacycle - Organic nitrogen compound - Primary alcohol - Alcohol - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic oxide - Organic oxygen compound - Amine - Organic cation - 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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