Compound Identification
SMILES
[H]\C(CC[C@](C)(O)[C@@]1([H])CC[C@]2(C)[C@]1([H])CC[C@]1([H])[C@@]3(C)CC[C@]([H])(O[C@]4([H])O[C@]([H])(CO)[C@@]([H])(O)[C@]([H])(O)[C@@]4([H])O[C@]4([H])OC[C@]([H])(O)[C@]([H])(O)[C@@]4([H])O)C(C)(C)[C@]3([H])C[C@]([H])(O)[C@@]21CO)=C(\C)CO
InChIKey
InChIKey=QYSPKCFUBCTSNU-XGXLZXSHSA-N
Formula
C41H70O14
Mass
786.997
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Lipids and lipid-like molecules
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Class
Prenol lipids
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Subclass
Terpene glycosides
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Level 5
Triterpene glycosides
- Level 6 Triterpene saponins
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Level 5
Triterpene glycosides
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Subclass
Terpene glycosides
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Class
Prenol lipids
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Prenol lipids
Subclass
Terpene glycosides
Intermediate Tree Nodes
Triterpene glycosides
Direct Parent
Triterpene saponins
Alternative Parents
Triterpenoids Steroidal glycosides 14-alpha-methylsteroids 7-alpha-hydroxysteroids Fatty acyl glycosides of mono- and disaccharides Alkyl glycosides Disaccharides O-glycosyl compounds Fatty alcohols Oxanes Tertiary alcohols Secondary alcohols Cyclic alcohols and derivatives Polyols Acetals Oxacyclic compounds Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Triterpene saponin - Triterpenoid - Steroidal glycoside - 26-hydroxysteroid - 20-hydroxysteroid - 14-alpha-methylsteroid - 7-hydroxysteroid - 7-alpha-hydroxysteroid - Hydroxysteroid - Steroid - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Disaccharide - Glycosyl compound - O-glycosyl compound - Fatty alcohol - Fatty acyl - Oxane - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Polyol - Organoheterocyclic compound - Acetal - Oxacycle - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton.
External Descriptors
Not available