Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCC(=O)NC1=NC(=O)N(C=C1F)[C@H]1C[C@H](O)[C@@H](COP(O)(=O)O[C@@H]2C[C@@H](CO)O[C@H]2N2C=C(F)C(=O)NC2=O)O1

InChIKey

InChIKey=HALVDEMJIVMWIO-WKWNQEBXSA-N

Formula

C36H56F2N5O12P

Mass

819.838

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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 - Pyrimidine 3'-deoxyribonucleoside - Pyrimidine nucleoside - N-arylamide - Halopyrimidine - Pyrimidone - Dialkyl phosphate - Aryl fluoride - Aryl halide - Fatty amide - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Imidolactam - Fatty acyl - Heteroaromatic compound - Vinylogous amide - Oxolane - Carboxamide group - Urea - Secondary carboxylic acid amide - Secondary alcohol - Lactam - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Oxacycle - Hydrocarbon derivative - Organohalogen compound - Carbonyl group - Organofluoride - Organonitrogen compound - Organooxygen compound - Primary alcohol - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organic oxide - 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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