CN(C)C1=CC=CC(CNC(=O)C2=CC3=C(SC(=N3)[C@@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)C=C2)=C1

InChIKey=PJLJBYOLAWJYCI-OBJCFNGXSA-N

C23H27N3O6S

473.54

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

2-pyranosylbenzothiazoles

Not available

2-pyranosylbenzothiazoles

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.

Not available