Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1[C@@H](O)[C@@H](C)O[C@H](O[C@@H]2[C@@H](O)[C@@H](O)[C@@H](C)O[C@@H]2O[C@@H]2[C@@H](O)[C@@H](O)[C@@H](C)O[C@H]2OC2=CC=CC3=C2C2=C4C(=C(N)C(=O)C5=C4C(=C(C)C=C5)C(=O)O2)C3=O)[C@@H]1O

InChIKey

InChIKey=GDNZKYXFSRQGRZ-UFVMVPLKSA-N

Formula

C39H43NO17

Mass

797.763

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

Not available

Direct Parent

Oligosaccharides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Oligosaccharide - Phenolic glycoside - Anthracene - Naphthopyran - Phenanthrene - Coumarin - Glycosyl compound - Isocoumarin - O-glycosyl compound - Benzopyran - 2-benzopyran - 1-benzopyran - Pyranone - Oxane - Benzenoid - Primary aromatic amine - Pyran - Vinylogous amide - Heteroaromatic compound - Secondary alcohol - Lactone - Acetal - Dialkyl ether - Organoheterocyclic compound - Oxacycle - Ether - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organic oxide - Organopnictogen compound - Primary amine - Amine - Alcohol - Aromatic heteropolycyclic 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

Previous Back Next