Structure Information
Structure

Compound Identification

SMILES

C[C@H]1C[C@@]2(C[C@H](C)[C@@H]3O[C@H](CC(=O)CCO)[C@H](O)C[C@@H]3O2)O[C@H]2C[C@]3(C[C@H]4O[C@H]5[C@H](C)[C@H]6OC(=O)C[C@H]7CC[C@@H]8O[C@H]9[C@@H]%10O[C@@]%11(C[C@H]%10O[C@H]9[C@@H](O%11)[C@H]8O7)CC[C@H]7CC(=C)[C@H](CC[C@H]8C[C@@H](C)C(=C)[C@@H](C[C@@H]6O[C@H]5C[C@H]4O3)O8)O7)O[C@@H]12

InChIKey

InChIKey=WVWWZNXKZNACRW-UJDDHLRZSA-N

Formula

C61H86O19

Mass

1123.34

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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

Glycosyl compounds

Direct Parent

C-glycosyl compounds

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

C-glycosyl compound - Disaccharide - Furopyran - Furofuran - Ketal - 1,3-dioxepane - 1,4-dioxepane - Dioxepane - Beta-hydroxy ketone - Pyran - Oxane - Furan - Oxolane - Lactone - Ketone - Secondary alcohol - Carboxylic acid ester - Monocarboxylic acid or derivatives - Ether - Acetal - Dialkyl ether - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Hydrocarbon derivative - Carbonyl group - Aldehyde - Alcohol - Primary alcohol - Organic oxide - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond.

External Descriptors

Not available

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