C[C@@H]1[C@@H](O)[C@]2(OC(C)=O)[C@H]([C@@H]3C=C(CO)C[C@@H]4[C@@H](C=C(C)C4=O)[C@@]13O)C2(C)C

InChIKey=WZYGIALDVOKLLL-CHCCALAZSA-N

C22H30O6

390.476

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Diterpenoids

Not available

Tigliane and ingenane diterpenoids

Rhamnofolane and daphnane diterpenoids Long-chain fatty alcohols Fatty alcohol esters Alpha-branched alpha,beta-unsaturated ketones Tertiary alcohols Enones Acryloyl compounds Secondary alcohols Ketones Cyclic alcohols and derivatives Carboxylic acid esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives

Aliphatic homopolycyclic compounds

Tigliane diterpenoid - Daphnane diterpenoid - Rhamnofolane diterpenoid - Long chain fatty alcohol - Fatty alcohol ester - Fatty alcohol - Fatty acyl - Alpha-branched alpha,beta-unsaturated-ketone - Alpha,beta-unsaturated ketone - Tertiary alcohol - Enone - Cyclic alcohol - Acryloyl-group - Secondary alcohol - Ketone - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homopolycyclic compound

This compound belongs to the class of organic compounds known as tigliane and ingenane diterpenoids. These are diterpenoids containing the tigliane or ingenane carbon skeleton. The tigliane skeleton is a tetracyclic ring that consists of the 4/7/6/3 ring junction. It is derived from casbane by 6,10- and 5,14-cyclizations and is a framework of phorbol. The ingenane skeleton is derived by rearrangement of tigliane.

Not available