CC(=O)O[C@@H]1C[C@H]2C(C)(C)C(O)CC[C@]2(C)[C@H]2CC[C@@]3(C)[C@H](OC(O)[C@H]4O[C@@]34[C@]12C)C1=COC=C1

InChIKey=WVWLZJICFMEPEX-IYXRYJJWSA-N

C28H40O7

488.621

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Triterpenoids

Not available

Limonoids

Naphthopyrans Naphthalenes 1,4-dioxepanes Pyrans Oxanes Heteroaromatic compounds Furans Secondary alcohols Carboxylic acid esters Hemiacetals Cyclic alcohols and derivatives Oxacyclic compounds Monocarboxylic acids and derivatives Epoxides Dialkyl ethers Hydrocarbon derivatives Carbonyl compounds Organic oxides

Aromatic heteropolycyclic compounds

Limonoid skeleton - Naphthopyran - Naphthalene - 1,4-dioxepane - Dioxepane - Oxane - Pyran - Cyclic alcohol - Furan - Heteroaromatic compound - Secondary alcohol - Carboxylic acid ester - Hemiacetal - Ether - Oxirane - Dialkyl ether - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Alcohol - Carbonyl group - 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