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Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H]([C@H](O)[C@@H](O)[C@H]1O)N1C2=C(C=C(F)C=C2)N=C1C1=CC=C(O1)[N+]([O-])=O

InChIKey

InChIKey=WOTSGGIUBKSMEP-QVXJJGPISA-N

Formula

C17H16FN3O8

Mass

409.326

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

1-pyranosylbenzimidazoles

Intermediate Tree Nodes

Not available

Direct Parent

1-pyranosylbenzimidazoles

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1-pyranosylbenzimidazole - Hexose monosaccharide - Glycosyl compound - N-glycosyl compound - Benzimidazole - Nitroaromatic compound - 2-nitrofuran - Aryl fluoride - Aryl halide - Monosaccharide - N-substituted imidazole - Oxane - Benzenoid - Azole - Furan - Heteroaromatic compound - Imidazole - Secondary alcohol - Organic nitro compound - C-nitro compound - Propargyl-type 1,3-dipolar organic compound - Polyol - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Oxacycle - Azacycle - Organic oxoazanium - Organoheterocyclic compound - Primary alcohol - Organohalogen compound - Organofluoride - Organic oxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organic zwitterion - Organooxygen compound - Organic salt - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 1-pyranosylbenzimidazoles. These are nucleoside and nucleotide analogs with a structure that consists of a Benzimidazole which is N-substituted at the 1-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.

External Descriptors

Not available

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