OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@H]1O)C1=NC2=C(S1)C=CC(=C2)C(=O)NCCN1CCNC1=O

InChIKey=UAWLWDVGLVXEJP-DZQJYWQESA-N

C19H24N4O7S

452.48

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

2-pyranosylbenzothiazoles

Not available

2-pyranosylbenzothiazoles

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

Aromatic heteropolycyclic compounds

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