Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1[C@@H](O)[C@@H](O[C@@H]1C(O[C@H]1OC(=C[C@H](O)[C@@H]1O)C(=O)NC1=CC(Cl)=C(F)C=C1)C(N)=O)N1C=CC(=O)NC1=O

InChIKey

InChIKey=HSDGIBKRVRENLA-OUVXQVHASA-N

Formula

C23H24ClFN4O11

Mass

586.91

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic oxygen compounds

Class

Organooxygen compounds

Subclass

Carbohydrates and carbohydrate conjugates

Intermediate Tree Nodes

Glycosyl compounds

Direct Parent

Glycosylamines

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Disaccharide - N-glycosyl compound - Anilide - N-arylamide - Chlorobenzene - Fluorobenzene - Halobenzene - Pyrimidone - Aryl chloride - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Hydropyrimidine - Pyrimidine - Benzenoid - Vinylogous amide - Oxolane - Heteroaromatic compound - Urea - Primary carboxylic acid amide - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Lactam - Organoheterocyclic compound - Oxacycle - Acetal - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organic nitrogen compound - Organochloride - Carbonyl group - Organonitrogen compound - Organopnictogen compound - Organofluoride - Organic oxide - Hydrocarbon derivative - Organohalogen compound - Alcohol - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).

External Descriptors

Not available

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