[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[C@@]2([H])[C@@]33C=CC[C@@]2(C)CN(CC)[C@]13[H]

InChIKey=LSVGXZONTJGRLJ-QDQDSUEZSA-N

C22H33NO3

359.51

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Diterpenoids

Not available

Aconitane-type diterpenoid alkaloids

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

Aliphatic heteropolycyclic compounds

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