Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCC(=O)OC[C@@H](COP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=C(F)C(N)=NC1=O)OC(=O)CCCCCCCCCCCCCCC

InChIKey

InChIKey=SSWWFQHKDZSUEY-DKJLCONMSA-M

Formula

C44H78FN3O12P

Mass

891.09

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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 - Aminopyrimidine - Fatty acid ester - Halopyrimidine - Pyrimidone - Dialkyl phosphate - Alkyl phosphate - Dicarboxylic acid or derivatives - Hydropyrimidine - Pyrimidine - Monosaccharide - Aryl halide - Phosphoric acid ester - Organic phosphoric acid derivative - Aryl fluoride - Imidolactam - Fatty acyl - Heteroaromatic compound - Oxolane - Secondary alcohol - Amino acid or derivatives - 1,2-diol - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Primary amine - Hydrocarbon derivative - Organic nitrogen compound - Alcohol - Organic oxygen compound - Amine - Organic oxide - Carbonyl group - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Organic anion - 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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