C[C@@]12CC[C@@H]3[C@@]4(C)C=CC(=O)OC(C)(C)[C@@H]4C[C@@H](O)[C@@]3(C)[C@]11O[C@@H]1[C@@H](O)[C@H]2C1=COC=C1

InChIKey=HERMHVZPYIFSGV-FMDORUDMSA-N

C26H34O6

442.552

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Triterpenoids

Not available

Limonoids

Naphthopyrans Naphthalenes Pyrans Oxanes Enoate esters Furans Heteroaromatic compounds Secondary alcohols Cyclic alcohols and derivatives Lactones Oxacyclic compounds Dialkyl ethers Epoxides Monocarboxylic acids and derivatives Carbonyl compounds 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 - Lactone - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Dialkyl ether - Oxirane - Ether - Monocarboxylic acid or derivatives - Carbonyl group - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organic oxide - 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