[H][C@]1(O)[C@@]2([H])C[C@@]3([H])[C@]1([H])[C@](O)(C[C@]2([H])OC)[C@@]1([H])[C@]([H])(OC)[C@@]2([H])[C@@]33C=CC(=O)[C@@]2(COC)CN(CC)[C@]13[H]

InChIKey=CODZZPSECBTZDT-CTMLWDBPSA-N

C24H35NO6

433.545

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Diterpenoids

Not available

Aconitane-type diterpenoid alkaloids

Quinolidines Alkaloids and derivatives Cyclohexenones Azepanes Piperidines Tertiary alcohols Trialkylamines Secondary alcohols Cyclic alcohols and derivatives Dialkyl ethers Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Aconitane-type diterpenoid alkaloid - Quinolidine - Alkaloid or derivatives - Azepane - Cyclohexenone - Piperidine - Cyclic alcohol - Tertiary alcohol - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Ketone - Organoheterocyclic compound - Azacycle - Dialkyl ether - Ether - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organopnictogen compound - Alcohol - Carbonyl group - Organic nitrogen compound - Amine - Hydrocarbon derivative - Aliphatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom.

Not available