Compound Identification
SMILES
COC(=O)C12OCC34C1C(OC(=O)C(C(C)O)=C(C)C)C(=O)OC3CC1=C(C)C(=O)C(O)=CC1(C)C4C(O)C2O
InChIKey
InChIKey=CFHBLZPGWLLCCS-UHFFFAOYSA-N
Formula
C28H34O12
Mass
562.568
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
-
Subclass
Terpene lactones
- Level 5 Quassinoids
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Subclass
Terpene lactones
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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 lactones
Intermediate Tree Nodes
Not available
Direct Parent
Quassinoids
Alternative Parents
Naphthopyranones Naphthalenes Tricarboxylic acids and derivatives Furopyrans Beta hydroxy acids and derivatives Delta valerolactones Pyranones and derivatives Fatty acid esters Oxepanes Oxanes Tetrahydrofurans Enoate esters Furans Methyl esters Cyclic ketones Cyclic alcohols and derivatives Secondary alcohols Polyols Enols Dialkyl ethers Oxacyclic compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Quassinoid - Naphthopyranone - Naphthopyran - Naphthalene - Furopyran - Tricarboxylic acid or derivatives - Beta-hydroxy acid - Delta valerolactone - Pyranone - Fatty acid ester - Oxepane - Delta_valerolactone - Fatty acyl - Pyran - Oxane - Hydroxy acid - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Methyl ester - Tetrahydrofuran - Cyclic alcohol - Furan - Cyclic ketone - Carboxylic acid ester - Secondary alcohol - Ketone - Lactone - Polyol - Ether - Enol - Dialkyl ether - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Alcohol - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring.
External Descriptors
Not available