CN(C)C1=CC=CC(CNC(=O)C2=CC3=C(C=C2)N=C(N3)[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)=C1

InChIKey=LSTGHUBYSIHSJR-XDWAVFMPSA-N

C23H28N4O6

456.499

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

2-pyranosylbenzimidazoles

Not available

2-pyranosylbenzimidazoles

Hexoses C-glycosyl compounds Benzimidazoles Dialkylarylamines Aniline and substituted anilines Oxanes Imidazoles Heteroaromatic compounds Secondary alcohols Secondary carboxylic acid amides 1,2-diols Amino acids and derivatives Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives Primary alcohols

Aromatic heteropolycyclic compounds

2-pyranosylbenzimidazole - Hexose monosaccharide - C-glycosyl compound - Glycosyl compound - Benzimidazole - Aniline or substituted anilines - Dialkylarylamine - Monosaccharide - Monocyclic benzene moiety - Oxane - Benzenoid - Imidazole - Azole - Heteroaromatic compound - Secondary alcohol - Secondary carboxylic acid amide - Tertiary amine - Carboxamide group - Amino acid or derivatives - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Polyol - Amine - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Primary alcohol - Hydrocarbon derivative - 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