Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OCCCCCCO[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=XQMMKUHZKAAKLO-ZMTFEQSMSA-N

Formula

C21H36N3O14P

Mass

585.5

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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

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Glycosyl compound - N-glycosyl compound - O-glycosyl compound - Monosaccharide phosphate - Aminopyrimidine - Dialkyl phosphate - Pyrimidone - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Oxane - Fatty acyl - Phosphoric acid ester - Primary aromatic amine - Imidolactam - Pyrimidine - Alkyl phosphate - Oxolane - Heteroaromatic compound - Secondary alcohol - Polyol - Organoheterocyclic compound - Acetal - Azacycle - Oxacycle - Organic oxygen compound - Alcohol - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - 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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