Structure Information
Structure

Compound Identification

SMILES

CCOC(=O)[C@H]1O[C@H](C[C@H]1O)[C@@]1(C)OC2(OC3(O[C@H]([C@@H](C)C(=O)[C@@H](C)[C@@H](O)[C@H](C)C[C@H](C)C4=C(C(O)=O)C(O)=C(CC)C=C4)[C@@H](C)C[C@H]3C)C=C[C@H]2O)[C@H](C)[C@H]1OC

InChIKey

InChIKey=AFGBEDQMTFPVJS-SFCKOIFTSA-N

Formula

C44H66O14

Mass

818.998

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Terpene glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Diterpene glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Diterpene glycoside - Diterpenoid - C-glycosyl compound - Glycosyl compound - P-cymene - Hydroxybenzoic acid - Pentose monosaccharide - Salicylic acid or derivatives - Salicylic acid - Benzoic acid or derivatives - Benzoic acid - Benzoyl - Beta-hydroxy acid - Phenol - 1-hydroxy-4-unsubstituted benzenoid - Ketal - Benzenoid - Monocyclic benzene moiety - Pyran - Beta-hydroxy ketone - Dicarboxylic acid or derivatives - Hydroxy acid - Monosaccharide - Oxane - Oxolane - Vinylogous acid - Secondary alcohol - Ketone - Carboxylic acid ester - Acetal - Oxacycle - Ether - Organoheterocyclic compound - Dialkyl ether - Carboxylic acid derivative - Carboxylic acid - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Aldehyde - Carbonyl group - Organooxygen compound - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated.

External Descriptors

Not available

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