Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCCOCC(COP(O)(=O)OC[C@H]1O[C@H]([C@@H](O)[C@@H]1O)N1C=CC(NC(=O)CCCCCCCCCCCCCCC)=NC1=O)OCCCCCCCCCCCCCCCCCC

InChIKey

InChIKey=RGUCVESUNXBITI-AOZRJBOGSA-N

Formula

C64H122N3O11P

Mass

1140.664

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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 - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Pentose monosaccharide - Glycerophospholipid - N-arylamide - Dialkyl phosphate - Glycerol ether - Pyrimidone - Fatty acyl - Imidolactam - Fatty amide - Alkyl phosphate - Hydropyrimidine - Monosaccharide - Pyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Heteroaromatic compound - Oxolane - Carboxamide group - Secondary carboxylic acid amide - 1,2-diol - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Carboxylic acid derivative - Azacycle - Carbonyl group - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Alcohol - Organonitrogen compound - Organooxygen compound - Organic oxide - 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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