Compound Identification
SMILES
CCC1(C)C(CCC2(C)C1CCC1(C)C2CC=C2C3CC(C)(C)C(OC4OC(CO)C(O)C(O)C4O)C(OC(C)=O)C3(CO)C(O)CC12C)OC1OC(C(OC(=O)C(C)=CC)C(O)C1OC(=O)C(C)=CC)C(O)=O
InChIKey
InChIKey=SYFLRMSFWBXNRJ-UHFFFAOYSA-N
Formula
C55H84O19
Mass
1049.258
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 16-oxosteroids 7-hydroxysteroids O-glucuronides Tetracarboxylic acids and derivatives O-glycosyl compounds Fatty acid esters Pyrans Oxanes Monosaccharides Enoate esters Secondary alcohols Cyclic alcohols and derivatives Oxacyclic compounds Polyols Carboxylic acids Acetals Primary alcohols Carbonyl compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Triterpene saponin - Triterpenoid - Hydroxysteroid - 16-oxosteroid - Oxosteroid - 7-hydroxysteroid - Steroid - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Tetracarboxylic acid or derivatives - Glycosyl compound - O-glycosyl compound - Fatty acid ester - Fatty acyl - Monosaccharide - Oxane - Pyran - Cyclic alcohol - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Secondary alcohol - Organoheterocyclic compound - Polyol - Carboxylic acid derivative - Carboxylic acid - Acetal - Oxacycle - Hydrocarbon derivative - Organooxygen compound - Organic oxygen compound - Carbonyl group - Primary alcohol - Alcohol - Organic oxide - 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