Compound Identification
SMILES
CC(C)C1(C)CCC(C)(O1)C1CCC2(C)C1CC(O)C1C3(C)CCC(=O)C(C)(C)C3CCC21C
InChIKey
InChIKey=XHIAVPAVQWVMAW-UHFFFAOYSA-N
Formula
C31H52O3
Mass
472.754
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 3-oxosteroids 11-hydroxysteroids Tetrahydrofurans Secondary alcohols Cyclic ketones Cyclic alcohols and derivatives Oxacyclic compounds Dialkyl ethers Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Triterpene saponin - Triterpenoid - 3-oxosteroid - Hydroxysteroid - Oxosteroid - 11-hydroxysteroid - Steroid - Cyclic alcohol - Tetrahydrofuran - Ketone - Secondary alcohol - Cyclic ketone - Oxacycle - Ether - Dialkyl ether - Organoheterocyclic compound - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - 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