CC(=O)O[C@@H]1C[C@H](OC(C)=O)[C@@]2(C)[C@H]3[C@@H](OC[C@]13C)[C@@H](O)[C@]1(C)[C@@H]2CC[C@@]2(C)[C@@H](OC(=O)[C@@H]3O[C@]123)C1=COC=C1

InChIKey=LVAGOWFLIUIEFT-LAFZNRGESA-N

C30H38O10

558.624

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Triterpenoids

Not available

Limonoids

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

Aromatic heteropolycyclic compounds

Limonoid skeleton - Naphthopyran - Naphthofuran - Naphthalene - Tricarboxylic acid or derivatives - 1,4-dioxepane - Delta valerolactone - Dioxepane - Delta_valerolactone - Pyran - Oxane - Tetrahydrofuran - Heteroaromatic compound - Cyclic alcohol - Furan - Secondary alcohol - Carboxylic acid ester - Lactone - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Oxirane - Ether - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Carbonyl group - 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