Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)C1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O.CCCCCCCCCCCCCCCCOCC(COP(O)(O)=O)OC(=O)CCCCCCCCCCCCCCC

InChIKey

InChIKey=FQVCEJJZXYIYFL-JZSUZKPPSA-N

Formula

C44H85N3O15P2

Mass

958.118

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Subclass

Pyrimidine ribonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine ribonucleoside monophosphates

Alternative Parents

Molecular Framework

Not available

Substituents

Pyrimidine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - 1-alkyl,2-acyl-glycerol-3-phosphate - Glycosyl compound - N-glycosyl compound - Sn-glycerol-3-phosphate - Monosaccharide phosphate - Pentose monosaccharide - Glycerophospholipid - Aminopyrimidine - Monoalkyl phosphate - Glycerol ether - Pyrimidone - Fatty acid ester - Fatty acyl - Alkyl phosphate - Imidolactam - Pyrimidine - Hydropyrimidine - Phosphoric acid ester - Monosaccharide - Organic phosphoric acid derivative - Heteroaromatic compound - Oxolane - Secondary alcohol - Carboxylic acid ester - 1,2-diol - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Monocarboxylic acid or derivatives - Carbonyl group - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Primary amine - Organic oxide - Alcohol - Amine - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine ribonucleoside monophosphates. These are pyrimidine ribobucleotides with monophosphate group linked to the ribose moiety.

External Descriptors

Not available

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