Nucleosides, nucleotides, and analogues
Nucleoside and nucleotide analogues
Intermediate Tree Nodes
Hexoses C-glycosyl compounds Benzothiazoles Chlorobenzenes Oxanes Aryl chlorides Thiazoles Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Dialkyl ethers Organochlorides Organonitrogen compounds Organic oxides Primary alcohols Hydrocarbon derivatives
Aromatic heteropolycyclic compounds
2-pyranosylbenzothiazole - Hexose monosaccharide - C-glycosyl compound - Glycosyl compound - 1,3-benzothiazole - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Oxane - Azole - Heteroaromatic compound - Thiazole - 1,2-diol - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Polyol - Oxacycle - Azacycle - Carboxylic acid derivative - Ether - Dialkyl ether - Organoheterocyclic compound - Organooxygen compound - Alcohol - Organic nitrogen compound - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Aromatic heteropolycyclic compound
This compound belongs to the class of organic compounds known as 2-pyranosylbenzothiazoles. These are nucleoside and nucleotide analogs with a structure that consists of a benzothiazole base 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.