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Structure Information
Structure

Compound Identification

SMILES

CC(=O)OC[C@H]1O[C@H]([C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O)N1C(SCC2=CC=C(C=C2)[N+]([O-])=O)=NC2=CC=CC=C12

InChIKey

InChIKey=IUUOFWVIZRCTLA-IURCNINISA-N

Formula

C28H29N3O11S

Mass

615.61

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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 - Tetracarboxylic acid or derivatives - Glycosyl compound - N-glycosyl compound - Nitrobenzene - Benzimidazole - Aryl thioether - Nitroaromatic compound - Alkylarylthioether - Oxane - Benzenoid - Monocyclic benzene moiety - N-substituted imidazole - Monosaccharide - Azole - Heteroaromatic compound - Imidazole - Carboxylic acid ester - C-nitro compound - Organic nitro compound - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Sulfenyl compound - Thioether - Organopnictogen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Organic oxygen compound - 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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