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=CN=C(Cl)C=C1

InChIKey=ZTZUYVCAGCUBMD-PLLDYVMSSA-N

C20H21ClN4O6

448.86

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

2-pyranosylbenzimidazoles

Not available

2-pyranosylbenzimidazoles

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

Aromatic heteropolycyclic compounds

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