Structure Information
Structure

Compound Identification

SMILES

[H][C@@]1(O)CO[C@]([H])(O[C@]2([H])[C@]([H])(O)[C@@]([H])(O)[C@]([H])(C)O[C@@]2([H])OC[C@@]2([H])O[C@@]([H])(OC3=C(C4=C(C=CN4C)C=C3)C3=CC4=C(OCO4)C=C3CO)[C@]([H])(O)[C@@]([H])(O)[C@]2([H])O)[C@]([H])(O)[C@@]1([H])O

InChIKey

InChIKey=UFKLWMRPZZKYNN-JATJOMADSA-N

Formula

C34H43NO17

Mass

737.708

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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

Aromatic heteropolycyclic compounds

Substituents

Oligosaccharide - Galanthindole-type amaryllidaceae alkaloid - Phenolic glycoside - Glycosyl compound - O-glycosyl compound - N-alkylindole - Benzodioxole - Indole - Indole or derivatives - Alkaloid or derivatives - N-methylpyrrole - Benzenoid - Substituted pyrrole - Oxane - Heteroaromatic compound - Pyrrole - Secondary alcohol - Polyol - Acetal - Organoheterocyclic compound - Azacycle - Oxacycle - Organonitrogen compound - Aromatic alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Alcohol - Primary 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

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