C[C@H]1C[C@H]2C=C(C)C[C@]34[C@@H](C)CC[C@H]1C23C(=O)C(C)=C(O)C4=O

InChIKey=CGNQDBPLJCEZON-PTTDNGFQSA-N

C20H26O3

314.425

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Diterpenoids

Not available

Elisapterane, elisabane, cumbiane or colombiane diterpenoids

Cyclohexenones Vinylogous acids Enols Organic oxides Hydrocarbon derivatives

Aliphatic homopolycyclic compounds

Elisapterane, elisabane, cumbiane or colombiane diterpenoid - Cyclohexenone - Vinylogous acid - Ketone - Enol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homopolycyclic compound

This compound belongs to the class of organic compounds known as elisapterane, elisabane, cumbiane or colombiane diterpenoids. These are diterpenoids with a structure based on either the elisapterane, elisabane, cumbiane or colombiane skeleton. They derive from serrulatane. Elisapterane is a tetracyclic compound formed by C10-C15 cyclization of elisabethane. Elisabane (nor-elisapterane) results from the loss of the C17 carbon atom of elisapterane. Cumbiane is formed by C10-C16 cyclization of the elisabethane carbon skeleton. Meanwhile, the cleavage of the C15-C16 bond of cumbiane yields the seco-cumbiane skeleton. Colombiane is also a tetracyclic skeleton arises from the C12-C2 cyclization of the elisabethane skeleton.

Not available