Compound Identification
SMILES
CC(=O)OC1CC2C(C)(C)C(=O)C3OC3C2(C)C2CCC3(C)C(C(=O)C4OC34C12C)C1=COC=C1
InChIKey
InChIKey=IRLGUCNVQLHFII-UHFFFAOYSA-N
Formula
C28H34O7
Mass
482.573
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
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Subclass
Triterpenoids
- Level 5 Limonoids
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Subclass
Triterpenoids
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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
Triterpenoids
Intermediate Tree Nodes
Not available
Direct Parent
Limonoids
Alternative Parents
Steroid esters 1,2-epoxy-3-oxosteroids Naphthopyranones Naphthalenes Pyranones and derivatives Oxepanes Oxanes Furans Heteroaromatic compounds Carboxylic acid esters Ketones Oxacyclic compounds Dialkyl ethers Monocarboxylic acids and derivatives Epoxides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Limonoid skeleton - Steroid ester - 1,2-epoxy-3-oxo-steroid - Oxosteroid - Steroid - Naphthopyranone - Naphthopyran - Naphthalene - Oxepane - Pyranone - Oxane - Pyran - Furan - Heteroaromatic compound - Ketone - Carboxylic acid ester - Monocarboxylic acid or derivatives - Ether - Oxirane - Dialkyl ether - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.
External Descriptors
Not available