Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CC(F)(F)P(O)(O)=O)[C@@H](OC(=O)C2=CC=CC=C2)[C@H]1OC(=O)C1=CC=CC=C1

InChIKey

InChIKey=PVPPLBFQMSVFTE-WGQQHEPDSA-N

Formula

C25H22F2N5O8P

Mass

589.449

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Benzoate ester - Benzoic acid or derivatives - Imidazopyrimidine - Purine - Benzoyl - Aminopyrimidine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Imidolactam - Pyrimidine - Benzenoid - Oxolane - Azole - Organophosphonic acid derivative - Organophosphonic acid - Heteroaromatic compound - Imidazole - Amino acid or derivatives - Carboxylic acid ester - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Oxacycle - Organic oxygen compound - Alkyl fluoride - Alkyl halide - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organofluoride - Organophosphorus compound - Organonitrogen compound - Primary amine - Amine - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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