Structure Information
Structure

Compound Identification

SMILES

CCCCCCCC\C=C/CCCCCCCC(=O)O[C@H]1C[C@@H](O[C@@H]1COP(O)(=O)OCC[N+](C)(C)C)N1C=C(F)C(=O)NC1=O

InChIKey

InChIKey=JLGWAGKPIWGUEH-NGLMKZPHSA-O

Formula

C32H56FN3O9P

Mass

676.784

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Subclass

Pyrimidine deoxyribonucleotides

Intermediate Tree Nodes

Pyrimidine deoxyribonucleoside monophosphates

Direct Parent

Pyrimidine 2'-deoxyribonucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside monophosphate - Phosphocholine - Fatty acid ester - Halopyrimidine - Pyrimidone - Dialkyl phosphate - Aryl fluoride - Aryl halide - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Fatty acyl - Quaternary ammonium salt - Tetraalkylammonium salt - Vinylogous amide - Oxolane - Heteroaromatic compound - Carboxylic acid ester - Urea - Lactam - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Oxacycle - Monocarboxylic acid or derivatives - Organohalogen compound - Organofluoride - Organonitrogen compound - Amine - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Organopnictogen compound - Organic nitrogen compound - Organic oxide - Organic cation - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleoside monophosphates. These are pyrimidine nucleotides with a monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.

External Descriptors

Not available

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