Structure Information
Structure

Compound Identification

SMILES

CC(C)C(NC(=O)C(C)OC1C(O)C(CO)OC(OCC2=CC=CC=C2)C1NC(C)=O)C(=O)NC(CCC(=O)NCCCC(=O)NC1=CC2=C(C=C1)N=C1N(C2)C(=O)C2=CC=CC=C12)C(N)=O

InChIKey

InChIKey=ANGLYMSGPVXRBY-UHFFFAOYSA-N

Formula

C47H58N8O12

Mass

927.025

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic oxygen compounds

Class

Organooxygen compounds

Subclass

Carbohydrates and carbohydrate conjugates

Intermediate Tree Nodes

Aminosaccharides

Direct Parent

N-acyl-alpha-hexosamines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Non-alpha peptide - Glycopeptidomimetic - Alpha-dipeptide - Indoloquinazoline - N-acyl-alpha-hexosamine - Glutamine or derivatives - Valine or derivatives - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Gamma amino acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Quinazolinamine - Diazanaphthalene - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Quinazoline - Isoindolone - Isoindoline - Indole - Isoindole or derivatives - Isoindole - N-arylamide - Monocyclic benzene moiety - Fatty amide - Fatty acyl - Benzenoid - Monosaccharide - N-acyl-amine - Oxane - Acetamide - Secondary carboxylic acid amide - Primary carboxylic acid amide - Secondary alcohol - Carboxamide group - Propargyl-type 1,3-dipolar organic compound - Amidine - Acetal - Carboxylic acid amidine - Organic 1,3-dipolar compound - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Organoheterocyclic compound - Azacycle - Organonitrogen compound - Organic oxide - Primary alcohol - Alcohol - Hydrocarbon derivative - Carbonyl group - Organopnictogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as n-acyl-alpha-hexosamines. These are carbohydrate derivatives containing a hexose moiety in which the oxygen atom is replaced by an n-acyl group.

External Descriptors

Not available

Previous Back Next