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)NCC1=CC(Cl)=CC(Cl)=C1

InChIKey=PBOSEJXVPPZCTP-ICBNADEASA-N

C21H21Cl2N3O6

482.31

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

2-pyranosylbenzimidazoles

Not available

2-pyranosylbenzimidazoles

Hexoses C-glycosyl compounds Benzimidazoles Dichlorobenzenes Oxanes Aryl chlorides Imidazoles Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Dialkyl ethers Hydrocarbon derivatives Organic oxides Organochlorides Organonitrogen compounds Primary alcohols

Aromatic heteropolycyclic compounds

2-pyranosylbenzimidazole - Hexose monosaccharide - Glycosyl compound - C-glycosyl compound - Benzimidazole - 1,3-dichlorobenzene - Halobenzene - Chlorobenzene - Monocyclic benzene moiety - Benzenoid - Aryl halide - Monosaccharide - Aryl chloride - Oxane - Azole - Imidazole - Heteroaromatic compound - 1,2-diol - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Polyol - Oxacycle - Azacycle - Ether - Carboxylic acid derivative - Dialkyl ether - Organoheterocyclic compound - Organochloride - Alcohol - Organic nitrogen compound - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organohalogen 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