Nucleosides, nucleotides, and analogues
Nucleoside and nucleotide analogues
Intermediate Tree Nodes
Glycosylamines Benzimidazoles Nitrofurans Nitroaromatic compounds Oxanes Benzenoids N-substituted imidazoles Monosaccharides Heteroaromatic compounds Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Polyols Oxacyclic compounds Organic oxoazanium compounds Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions Organonitrogen compounds Primary alcohols
Aromatic heteropolycyclic compounds
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
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.