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Structure Information
Structure

Compound Identification

SMILES

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

InChIKey=PJLJBYOLAWJYCI-OBJCFNGXSA-N

Formula

C23H27N3O6S

Mass

473.54

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

2-pyranosylbenzothiazoles

Intermediate Tree Nodes

Not available

Direct Parent

2-pyranosylbenzothiazoles

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

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

Description

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.

External Descriptors

Not available

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