You are using an unsupported browser. Please upgrade your browser to a newer version to get the best experience on ClassyFire.
Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H]([C@H](O)[C@@H](O)[C@@H]1O)N1C2=CC=CC=C2N=C1C1=CC=C(O1)[N+]([O-])=O

InChIKey

InChIKey=FJYZSZLTWBWBQZ-AQFIFQLPSA-N

Formula

C17H17N3O8

Mass

391.336

Export to:

JSON SDF CSV

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

Previous Back Next