OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@H]1O)C1=NC2=C(S1)C=CC(=C2)C(=O)NC1=CC(Cl)=CC=C1

InChIKey=XGQFTZKRHRMLPE-PLLDYVMSSA-N

C20H19ClN2O6S

450.89

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

2-pyranosylbenzothiazoles

Not available

2-pyranosylbenzothiazoles

Aromatic anilides Hexoses C-glycosyl compounds Benzothiazoles Chlorobenzenes Aryl chlorides Oxanes Thiazoles Heteroaromatic compounds Secondary alcohols Secondary carboxylic acid amides 1,2-diols Dialkyl ethers Azacyclic compounds Oxacyclic compounds Organochlorides 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 - Chlorobenzene - Monosaccharide - Benzenoid - Aryl halide - Oxane - Aryl chloride - Monocyclic benzene moiety - Azole - Thiazole - Heteroaromatic compound - 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.

Not available