Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1[C@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@H](O)[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](C)O[C@@H](O[C@@H]4[C@@H](O)[C@@H](CO[C@H]4O[C@H]4CC[C@@]5(C)[C@H](CC[C@@H]6C5=C[C@H](O)[C@]57C(=O)O[C@@](C)([C@H](O)CC=C(C)C)[C@@]5(O)CC[C@@]67C)C4(C)C)OS([O-])(=O)=O)[C@H](O)[C@H]3O)[C@@H]2O)[C@@H]1O

InChIKey

InChIKey=RPXDYBJJIRQTPW-XQRGYZGLSA-M

Formula

C54H85O27S

Mass

1198.31

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Triterpenoids

Intermediate Tree Nodes

Not available

Direct Parent

Triterpenoids

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Triterpenoid - Steroidal glycoside - Oligosaccharide - 22-hydroxysteroid - Steroid lactone - 12-hydroxysteroid - Hydroxysteroid - 17-hydroxysteroid - Steroid - Glycosyl compound - O-glycosyl compound - Sulfate-ester - Sulfuric acid monoester - Sulfuric acid ester - Alkyl sulfate - Oxane - Gamma butyrolactone - Tertiary alcohol - Tetrahydrofuran - Cyclic alcohol - Organic sulfuric acid or derivatives - Secondary alcohol - Carboxylic acid ester - Lactone - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Acetal - Monocarboxylic acid or derivatives - Carbonyl group - Primary alcohol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Organooxygen compound - Organic anion - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

External Descriptors

Not available

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