CC[C@H](C)[C@@H](O)C(=O)O[C@H]1[C@@H](OC=O)[C@@H](C(=C)[C@@]2(O)C(=O)C[C@@H](c3ccoc3)[C@]12C)[C@]1(C)[C@@H]2CC(=O)OC[C@@]2(C)OC(=O)C[C@@H]1OC(C)=O

InChIKey=FEQMUAOUKSLIFS-SKIIIRSQSA-N

C35H44O14

688.723

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Triterpenoids

Not available

Limonoids

Pentacarboxylic acids and derivatives Delta valerolactones Fatty acid esters Oxepanes Monosaccharides Oxanes Heteroaromatic compounds Furans Tertiary alcohols Carboxylic acid esters Ketones Secondary alcohols Cyclic alcohols and derivatives Oxacyclic compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Limonoid skeleton - Pentacarboxylic acid or derivatives - Caprolactone - Delta valerolactone - Fatty acid ester - Delta_valerolactone - Oxepane - Monosaccharide - Oxane - Fatty acyl - Tertiary alcohol - Cyclic alcohol - Furan - Heteroaromatic compound - Secondary alcohol - Carboxylic acid ester - Lactone - Ketone - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Alcohol - Organooxygen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organic oxygen 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