OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@H]1O)C1=NC2=C(N1)C=C(C=C2)C(=O)NC1=CC=C(OC2=CC=CC=C2)C=C1

InChIKey=GUCHKPJUVGXNRR-OYTPZHDJSA-N

C26H25N3O7

491.5

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

2-pyranosylbenzimidazoles

Not available

2-pyranosylbenzimidazoles

Aromatic anilides Diphenylethers Hexoses C-glycosyl compounds Diarylethers Benzimidazoles Phenoxy compounds Phenol ethers Oxanes Imidazoles Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Dialkyl ethers Organonitrogen compounds Organic oxides Primary alcohols Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

2-pyranosylbenzimidazole - Aromatic anilide - Diphenylether - Hexose monosaccharide - Glycosyl compound - Diaryl ether - C-glycosyl compound - Benzimidazole - Phenoxy compound - Phenol ether - Oxane - Benzenoid - Monosaccharide - Monocyclic benzene moiety - Heteroaromatic compound - Imidazole - Azole - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Carboxylic acid derivative - Dialkyl ether - Organoheterocyclic compound - Ether - Polyol - Alcohol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as 2-pyranosylbenzimidazoles. These are nucleoside and nucleotide analogs with a structure that consists of a benzimidazole which is N-substituted at the 2-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.

Not available