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=FJYZSZLTWBWBQZ-FUAJKEFHSA-N

C17H17N3O8

391.336

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

1-pyranosylbenzimidazoles

Not available

1-pyranosylbenzimidazoles

Glycosylamines Benzimidazoles Nitroaromatic compounds Nitrofurans Benzenoids Oxanes Monosaccharides N-substituted imidazoles Heteroaromatic compounds 1,2-diols Secondary alcohols Oxacyclic compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Organic oxides Organic salts Organic zwitterions Organonitrogen compounds Hydrocarbon derivatives Primary alcohols

Aromatic heteropolycyclic compounds

1-pyranosylbenzimidazole - Glycosyl compound - N-glycosyl compound - Benzimidazole - Nitroaromatic compound - 2-nitrofuran - Oxane - Benzenoid - Monosaccharide - N-substituted imidazole - Azole - Furan - Heteroaromatic compound - Imidazole - C-nitro compound - Organic nitro compound - 1,2-diol - Secondary alcohol - 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 - Polyol - Organic oxygen compound - Organic salt - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Alcohol - 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.

Not available