Structure Information
Structure

Compound Identification

SMILES

CN(C)CCCNC(=O)C1=CC(NC(=O)C2=CC(NC(=O)C3=C(C)N=C(N)S3)=CN2[C@H]2O[C@H](CO)[C@@H](O)[C@@H](O)[C@H]2O)=CN1[C@H]1O[C@H](CO)[C@@H](O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=WKHZIIBHZZCIRV-ULQKGGRHSA-N

Formula

C32H46N8O13S

Mass

782.82

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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

N-glycosyl compound - 2-heteroaryl carboxamide - 2,4,5-trisubstituted 1,3-thiazole - Pyrrole-2-carboxamide - Pyrrole-2-carboxylic acid or derivatives - Thiazolecarboxamide - Thiazolecarboxylic acid or derivatives - Monosaccharide - Oxane - 1,3-thiazol-2-amine - Substituted pyrrole - Azole - Heteroaromatic compound - Pyrrole - Thiazole - Secondary carboxylic acid amide - Secondary alcohol - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Carboxamide group - Azacycle - Oxacycle - Polyol - Organoheterocyclic compound - Carboxylic acid derivative - Amine - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Alcohol - Primary alcohol - Primary amine - 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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