Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=OPMRNRCEULVCQH-NHMWVPOYSA-N

Formula

C34H43F3N4O12

Mass

756.729

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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 - Trifluoromethylbenzene - Anilide - N-arylamide - Fatty acid ester - Pyrimidone - Monocyclic benzene moiety - Hydropyrimidine - Fatty acyl - Pyrimidine - Benzenoid - Heteroaromatic compound - Oxolane - Vinylogous amide - 1,2-diol - Carboxamide group - Carboxylic acid ester - Lactam - Primary carboxylic acid amide - Urea - Secondary alcohol - Secondary carboxylic acid amide - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Azacycle - Oxacycle - Acetal - Carboxylic acid derivative - Ether - Dialkyl ether - Carbonyl group - Organopnictogen compound - Alcohol - Organic oxide - Hydrocarbon derivative - Organofluoride - Organonitrogen compound - Alkyl fluoride - Alkyl halide - Organohalogen compound - Organic nitrogen compound - 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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