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)OC(=O)CCCCCCCCCCCCCCC

InChIKey

InChIKey=FIVNNPQCAUXOPI-FKTVNPGJSA-N

Formula

C62H116N3O12P

Mass

1126.593

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