Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCCOC(COP(O)(=O)OCC1OC(CC1O)N1C=C(F)C(=O)NC1=O)COP(O)(=O)OCC1OC(CC1N=[N+]=[N-])N1C=C(C)C(=O)NC1=O

InChIKey

InChIKey=SIHLTXWKMAYBQH-UHFFFAOYSA-N

Formula

C40H66FN7O16P2

Mass

981.947

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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 - Halopyrimidine - Pyrimidone - Glycerol ether - Dialkyl phosphate - Aryl fluoride - Aryl halide - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Oxolane - Vinylogous amide - Heteroaromatic compound - Urea - Secondary alcohol - Azo imide - Azo compound - Lactam - Dialkyl ether - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Hydrocarbon derivative - Organic oxide - Organohalogen compound - Alcohol - Organic nitrogen compound - Organofluoride - Organonitrogen compound - Organic salt - Organooxygen compound - Organic oxygen compound - 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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