Structure Information
Structure

Compound Identification

SMILES

CCCC(O[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1)C(C)C(O)C(CC)\C=C\C(O)C(C)C1C\C=C(C)\C(O)C(C)C(CC(O)C(C)C(O)CC2CC(O)C(O)C(O)(CC(O[C@@H]3O[C@H](C)[C@@H](O)[C@H](O[C@H]4C[C@@H](N)[C@H](O)[C@@H](C)O4)[C@H]3O[C@@H]3O[C@H](C)[C@@H](O)[C@H](O)[C@H]3O)C(C)CCC(O)CC(O)C\C=C(CC)\C(=O)O1)O2)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O

InChIKey

InChIKey=VJKZKLDZOAFAEE-QIESNYARSA-N

Formula

C81H144N2O33

Mass

1674.024

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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

Aliphatic heteropolycyclic compounds

Substituents

Diterpene glycoside - Aminoglycoside core - Diterpene lactone - Diterpenoid - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Macrolide - Alkyl glycoside - Disaccharide - Glycosyl compound - O-glycosyl compound - Amino saccharide - Fatty acyl - Oxane - Alpha,beta-unsaturated carboxylic ester - Enoate ester - 1,2-aminoalcohol - Amino acid or derivatives - Carboxylic acid ester - Secondary alcohol - Hemiacetal - Lactone - Polyol - Monocarboxylic acid or derivatives - Acetal - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Alcohol - Carbonyl group - Organic oxygen compound - Primary amine - Primary alcohol - Primary aliphatic amine - Organic nitrogen compound - Amine - Organonitrogen compound - Aliphatic 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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