Structure Information
Structure

Compound Identification

SMILES

CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@H](O)[C@@H](CO)O[C@@H](O[C@H]3[C@H](O)[C@@H](O)[C@H](O[C@H]4[C@H](O)[C@@H](CO)O[C@@H](O[C@H]5[C@H](O)[C@@H](O)[C@H](O[C@H]6[C@H](O)[C@@H](CO)O[C@@H](O[C@H]7[C@H](O)[C@@H](O)[CH+]O[C@@H]7C(O)=O)[C@@H]6NC(C)=O)O[C@@H]5C(O)=O)[C@@H]4NC(C)=O)O[C@@H]3C(O)=O)[C@@H]2NC(C)=O)O[C@@H]1C(O)=O

InChIKey

InChIKey=KKXJJVVETVJQOE-JJQHVIKWSA-O

Formula

C56H85N4O44

Mass

1518.279

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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

Not available

Direct Parent

Oligosaccharides

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

Oligosaccharide - N-acyl-alpha-hexosamine - Fatty acyl glycoside - 1-o-glucuronide - O-glucuronide - Tetracarboxylic acid or derivatives - Glucuronic acid or derivatives - O-glycosyl compound - Glycosyl compound - Fatty acyl - Oxane - Pyran - Acetamide - Secondary carboxylic acid amide - Carboxamide group - Secondary alcohol - Organoheterocyclic compound - Acetal - Oxacycle - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Alcohol - Organonitrogen compound - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic cation - Aliphatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

External Descriptors

Not available

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