CC(=O)OC1C(O)C2C(CCC3(C)C(CC=C23)C2=COC=C2)[C@@]2(C)CCC(=O)C(C)(C)C12

InChIKey=YFUNBQADJMJQLI-UPQHSBKYSA-N

C27H36O5

440.58

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Triterpenoids

Not available

Limonoids

17-furanylsteroids and derivatives Steroid esters 7-hydroxysteroids 3-oxosteroids Heteroaromatic compounds Furans Secondary alcohols Cyclic ketones Cyclic alcohols and derivatives Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Limonoid skeleton - 17-furanylsteroid skeleton - Steroid ester - 7-hydroxysteroid - Oxosteroid - Hydroxysteroid - 3-oxosteroid - Steroid - Heteroaromatic compound - Furan - Cyclic alcohol - Cyclic ketone - Secondary alcohol - Ketone - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - 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