Structure Information
Structure

Compound Identification

SMILES

CC(C)CCCCCCC\C=C\C(=O)N[C@@H]1[C@@H](O)[C@@H](O)[C@@H](C[C@H](O)[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(=O)NC2=O)O[C@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1NC(C)=O

InChIKey

InChIKey=FIIRBPHYBLFBSD-MSALFBPISA-N

Formula

C36H58N4O16

Mass

802.872

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 heteromonocyclic compounds

Substituents

N-acyl-alpha-hexosamine - Disaccharide - Glycosyl compound - N-glycosyl compound - O-glycosyl compound - Pyrimidone - Hydropyrimidine - N-acyl-amine - Oxane - Pyrimidine - Heteroaromatic compound - Acetamide - Oxolane - Vinylogous amide - Urea - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Lactam - Organoheterocyclic compound - Carboxylic acid derivative - Acetal - Oxacycle - Azacycle - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Primary alcohol - Hydrocarbon derivative - Organonitrogen compound - Carbonyl group - Alcohol - Aromatic heteromonocyclic 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