Structure Information
Structure

Compound Identification

SMILES

CCC(C1OC(CC)(CC1C)C1CCC(O)(CC)C(C)O1)C(=O)C(\C)=C\C(C)CCC1=C(Br)C=C(C)C(O)=C1C(O)=O

InChIKey

InChIKey=MELWHTUUZJGRLO-CAPFRKAQSA-N

Formula

C34H51BrO7

Mass

651.679

Export to:

JSON SDF CSV

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 heteromonocyclic compounds

Substituents

Diterpene glycoside - Diterpenoid - Hydroxybenzoic acid - Salicylic acid or derivatives - Salicylic acid - 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Halobenzoic acid - 3-halobenzoic acid - Benzoic acid - Benzoic acid or derivatives - 4-halophenol - Benzoyl - O-cresol - 4-bromophenol - Phenol - Halobenzene - Toluene - Bromobenzene - Alpha-branched alpha,beta-unsaturated-ketone - Benzenoid - Oxane - Aryl bromide - Monocyclic benzene moiety - Aryl halide - Vinylogous acid - Enone - Acryloyl-group - Tertiary alcohol - Oxolane - Alpha,beta-unsaturated ketone - Ketone - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Ether - Organobromide - Organooxygen compound - Alcohol - Organohalogen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteromonocyclic 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

Previous Back Next