CC(=O)OC[C@H]1O[C@H]([C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O)N1C(=S)NC2=CC=CC=C12

InChIKey=LUDJONSOAAVRLR-OUUBHVDSSA-N

C21H24N2O9S

480.49

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

1-pyranosylbenzimidazoles

Not available

1-pyranosylbenzimidazoles

Tetracarboxylic acids and derivatives Glycosylamines Benzimidazoles Benzenoids Oxanes Imidazolethiones N-substituted imidazoles Monosaccharides Heteroaromatic compounds Thioureas Carboxylic acid esters Azacyclic compounds Oxacyclic compounds Organonitrogen compounds Organopnictogen compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

1-pyranosylbenzimidazole - Tetracarboxylic acid or derivatives - Glycosyl compound - N-glycosyl compound - Benzimidazole - Imidazole-2-thione - Monosaccharide - Benzenoid - Oxane - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Carboxylic acid ester - Thiourea - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organosulfur compound - Organonitrogen compound - Organooxygen compound - 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