Compound Identification
SMILES
C[C@@]1(CC[C@H]2C(=C1)C(=O)C[C@H]1[C@@](C)(CO[C@@H]3O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]3O)[C@@H](O)[C@H](O)C[C@]21C)C=C
InChIKey
InChIKey=QPUZIMJVFNBYQT-JHSKIDNSSA-N
Formula
C26H40O9
Mass
496.597
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Steroids and steroid derivatives
- Subclass Steroidal glycosides
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Class
Steroids and steroid derivatives
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Steroids and steroid derivatives
Subclass
Steroidal glycosides
Intermediate Tree Nodes
Not available
Direct Parent
Steroidal glycosides
Alternative Parents
Diterpene glycosides 12-beta-hydroxysteroids Diterpenoids Hydrophenanthrenes Hexoses O-glycosyl compounds Oxanes Ketones Secondary alcohols Cyclic alcohols and derivatives Oxacyclic compounds Polyols Acetals Hydrocarbon derivatives Primary alcohols Organic oxides
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Diterpene glycoside - Steroidal glycoside - Diterpenoid - Pimarane diterpenoid - 12-beta-hydroxysteroid - 12-hydroxysteroid - Hydroxysteroid - Terpene glycoside - Hydrophenanthrene - Phenanthrene - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Oxane - Monosaccharide - Cyclic alcohol - Secondary alcohol - Ketone - Oxacycle - Organoheterocyclic compound - Acetal - Polyol - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Primary alcohol - Carbonyl group - Organooxygen compound - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton.
External Descriptors
Not available