Structure Information
Structure

Compound Identification

SMILES

CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC2=C(C=C1)N=C(C1=CC=CC=C1)C(=N2)C1=CC=C(CN2CCC(CC2)N2C(=O)NC3=CC=CC=C23)C=C1

InChIKey

InChIKey=VNNVBJURLDZKJG-FWDCKUSFSA-N

Formula

C41H42N6O7

Mass

730.822

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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

Aminosaccharides

Direct Parent

N-acyl-alpha-hexosamines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

N-acyl-alpha-hexosamine - N-benzylpiperidine - Benzylpiperidine - O-glycosyl compound - Glycosyl compound - Diazanaphthalene - Quinoxaline - Benzimidazole - Phenylmethylamine - Benzylamine - Aralkylamine - Piperidine - Pyrazine - Monocyclic benzene moiety - Oxane - Benzenoid - N-substituted imidazole - Monosaccharide - Heteroaromatic compound - Azole - Acetamide - Imidazole - Secondary alcohol - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Urea - Carboxamide group - Amino acid or derivatives - Acetal - Oxacycle - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Carbonyl group - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Amine - Organic nitrogen compound - Primary alcohol - Organonitrogen 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

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