Compound Identification
SMILES
CC[C@H]1[C@H](C[C@H]2[C@@H]3CC[C@H]4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)O[C@@H]1OC(CO)[C@H](O[C@@H]2OC(CO)[C@@H](O)[C@H](O[C@@H]3OC(CO)[C@@H](O)[C@H](O)C3O)C2O[C@@H]2OC(CO)[C@@H](O)[C@H](O[C@@H]3OC(C)[C@H](O)C(O)[C@@H]3O)C2O)[C@H](O)C1O)O[C@@]1(C)CC[C@@H](C)CO1
InChIKey
InChIKey=JHSZDVZYOFZGJV-CKCOFUPGSA-N
Formula
C58H98O27
Mass
1227.395
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Steroids and steroid derivatives
-
Subclass
Steroidal glycosides
- Level 5 Steroidal saponins
-
Subclass
Steroidal glycosides
-
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 saponins
Alternative Parents
Triterpenoids Spirostanes and derivatives Oligosaccharides O-glycosyl compounds Ketals Oxanes Secondary alcohols Polyols Oxacyclic compounds Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Steroidal saponin - Triterpenoid - Spirostane skeleton - Oligosaccharide - Glycosyl compound - O-glycosyl compound - Ketal - Oxane - Secondary alcohol - Polyol - Acetal - Oxacycle - Organoheterocyclic compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organic oxygen compound - Alcohol - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative.
External Descriptors
LIPIDMAPS (LMST01080076) : Spirostanols and derivatives