Compound Identification
SMILES
CC(C)(O)[C@H]1CC[C@](C)(O1)C1[C@@H](O)C[C@@]2(C)C3CCC4[C@]5(C[C@@]35CC[C@]12C)C=C\C(=N/O)C4(C)C
InChIKey
InChIKey=OTULGTWVXCAMCA-DKRPQAQNSA-N
Formula
C30H47NO4
Mass
485.709
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 Cycloartanols and derivatives 16-beta-hydroxysteroids Delta-1-steroids Tetrahydrofurans Tertiary alcohols Ketoximes Secondary alcohols Cyclic alcohols and derivatives Oxacyclic compounds Dialkyl ethers Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Triterpene saponin - 9b,19-cyclo-lanostane-skeleton - Triterpenoid - Hydroxysteroid - 16-beta-hydroxysteroid - 16-hydroxysteroid - Delta-1-steroid - Steroid - Tetrahydrofuran - Tertiary alcohol - Cyclic alcohol - Ketoxime - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Oxime - Dialkyl ether - Ether - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Alcohol - Organic nitrogen compound - Organopnictogen compound - 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