C[C@H]1C[C@H](C=C(C)C)C2=C3[C@@H]1CC[C@H](C)C3=C(OC(C)=O)C(O[C@H]1OC[C@H](O)C(O)C1O)=C2C

InChIKey=CFEIHTABPZLNQZ-TWXVBUIFSA-N

C27H38O7

474.594

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Diterpenoids

Not available

Amphilectane, neoamphilectane, cycloamphilectane, and adociane diterpenoids

Phenolic glycosides O-glycosyl compounds Tetralins Oxanes Monosaccharides Secondary alcohols Carboxylic acid esters Polyols Oxacyclic compounds Monocarboxylic acids and derivatives Acetals Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Amphilectane, neoamphilectane, cycloamphilectane, or adociane diterpenoid - Phenolic glycoside - Glycosyl compound - O-glycosyl compound - Tetralin - Monosaccharide - Oxane - Benzenoid - Secondary alcohol - Carboxylic acid ester - Polyol - Acetal - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Hydrocarbon derivative - Alcohol - Organooxygen compound - Organic oxide - Organic oxygen compound - Carbonyl group - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as amphilectane, neoamphilectane, cycloamphilectane, and adociane diterpenoids. These are diterpenoids with a structure based on the amphilectane or a seco-,neo-, or cyclo- derivative thereof. Amphilectane is a tricyclic structure made up of three cyclohexane fused together, with a methyl group at the C11-, C7-, and C3- positions. Additionally, it carries a 2-methylpropyl group at the C1-position. Amphilectanes are presumably derived from serrulatanes. Cycloamphilectanes represent a further cyclisation.

Not available