CCN(CC)C(=O)C1=CC2=C(SC(=N2)[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)C=C1

InChIKey=JFZQUUNPVVQABB-DZQJYWQESA-N

C18H24N2O6S

396.46

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

2-pyranosylbenzothiazoles

Not available

2-pyranosylbenzothiazoles

Hexoses C-glycosyl compounds Benzothiazoles Oxanes Benzenoids Thiazoles Tertiary carboxylic acid amides Heteroaromatic compounds Tertiary amines Secondary alcohols 1,2-diols Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Dialkyl ethers Hydrocarbon derivatives Organic oxides Primary alcohols

Aromatic heteropolycyclic compounds

2-pyranosylbenzothiazole - Hexose monosaccharide - C-glycosyl compound - Glycosyl compound - 1,3-benzothiazole - Monosaccharide - Oxane - Benzenoid - Heteroaromatic compound - Thiazole - Tertiary carboxylic acid amide - Azole - Tertiary amine - Secondary alcohol - Amino acid or derivatives - 1,2-diol - Carboxamide group - Oxacycle - Azacycle - Polyol - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Dialkyl ether - Amine - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Alcohol - 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.

Not available