CC12CCC3C4(C)C=CC(=O)OC(C)(C)C4C(O)C(=O)C3(C)C11OC1CC2C1=COC=C1

InChIKey=KXIBKDPQXSWDJM-UHFFFAOYSA-N

C26H32O6

440.536

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Triterpenoids

Not available

Limonoids

Naphthopyrans Naphthalenes Pyrans Oxanes Enoate esters Furans Heteroaromatic compounds Cyclic alcohols and derivatives Secondary alcohols Ketones Lactones Oxacyclic compounds Dialkyl ethers Epoxides Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Limonoid skeleton - Naphthopyran - Naphthalene - Oxane - Pyran - Cyclic alcohol - Furan - Heteroaromatic compound - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxylic acid ester - Secondary alcohol - Ketone - Lactone - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Dialkyl ether - Oxirane - Ether - Monocarboxylic acid or derivatives - Carbonyl group - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Aromatic heteropolycyclic compound

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.

Not available