Nucleosides, nucleotides, and analogues
Nucleoside and nucleotide analogues
Intermediate Tree Nodes
Hexoses C-glycosyl compounds Benzothiazoles Dialkylarylamines Aniline and substituted anilines Oxanes Heteroaromatic compounds Thiazoles Secondary carboxylic acid amides 1,2-diols Amino acids and derivatives Secondary alcohols Oxacyclic compounds Dialkyl ethers Azacyclic compounds Primary alcohols Organic oxides Hydrocarbon derivatives
Aromatic heteropolycyclic compounds
2-pyranosylbenzothiazole - Hexose monosaccharide - C-glycosyl compound - Glycosyl compound - 1,3-benzothiazole - Aniline or substituted anilines - Dialkylarylamine - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Oxane - Azole - Heteroaromatic compound - Thiazole - 1,2-diol - Amino acid or derivatives - Carboxamide group - Tertiary amine - Secondary alcohol - Secondary carboxylic acid amide - Polyol - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Dialkyl ether - Carboxylic acid derivative - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Alcohol - Organonitrogen compound - Primary alcohol - 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.