Structure Information
Structure

Compound Identification

SMILES

OC[C@@H]1OC[C@@H](O1)N1C=C(F)C(NC(=O)C2=CC=C(C=C2)[N+]([O-])=O)=NC1=O

InChIKey

InChIKey=YMSCFQLIRHGQOF-VXGBXAGGSA-N

Formula

C15H13FN4O7

Mass

380.288

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Nucleoside and nucleotide analogues

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Benzamide - Benzoic acid or derivatives - Nitrobenzene - Nitroaromatic compound - Benzoyl - Halopyrimidine - Pyrimidone - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Hydropyrimidine - Imidolactam - Pyrimidine - Benzenoid - Meta-dioxolane - Heteroaromatic compound - Carboxamide group - Organic nitro compound - C-nitro compound - Secondary carboxylic acid amide - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Oxacycle - Azacycle - Organic oxoazanium - Carboxylic acid derivative - Acetal - Organoheterocyclic compound - Primary alcohol - Alcohol - Organic salt - Organohalogen compound - Organic nitrogen compound - Organofluoride - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organic zwitterion - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as nucleoside and nucleotide analogues. These are analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others.

External Descriptors

Not available

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