Nucleosides, nucleotides, and analogues
Nucleoside and nucleotide analogues
Intermediate Tree Nodes
Aromatic anilides Hexoses C-glycosyl compounds Benzothiazoles Fluorobenzenes Aryl fluorides Oxanes Thiazoles Heteroaromatic compounds Secondary alcohols Secondary carboxylic acid amides 1,2-diols Dialkyl ethers Azacyclic compounds Oxacyclic compounds Organofluorides Organic oxides Hydrocarbon derivatives Primary alcohols Organonitrogen compounds
Aromatic heteropolycyclic compounds
2-pyranosylbenzothiazole - Aromatic anilide - Hexose monosaccharide - Glycosyl compound - C-glycosyl compound - 1,3-benzothiazole - Halobenzene - Fluorobenzene - Monosaccharide - Benzenoid - Aryl halide - Oxane - Aryl fluoride - Monocyclic benzene moiety - Azole - Thiazole - Heteroaromatic compound - 1,2-diol - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Polyol - Oxacycle - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Ether - Dialkyl ether - Organooxygen compound - Alcohol - Organic nitrogen compound - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organohalogen compound - Organofluoride - 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.