Compound Identification
SMILES
COC1CC2(O)C3CC4C5CCC(OC)C4(C4CC1C(O)C24)C3NC5=O
InChIKey
InChIKey=YSXNUVPIHIVGEE-UHFFFAOYSA-N
Formula
C20H29NO5
Mass
363.454
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
- Subclass Diterpenoids
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Class
Prenol lipids
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Prenol lipids
Subclass
Diterpenoids
Intermediate Tree Nodes
Not available
Direct Parent
Lappaconitine-type diterpenoid alkaloids
Alternative Parents
Quinolidines Alkaloids and derivatives Caprolactams Piperidinones Azepanes Delta lactams Tertiary alcohols Secondary carboxylic acid amides Secondary alcohols Cyclic alcohols and derivatives Azacyclic compounds Dialkyl ethers Carbonyl compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Lappaconitine-type diterpenoid alkaloid - Quinolidine - Alkaloid or derivatives - Caprolactam - Azepane - Delta-lactam - Piperidinone - Piperidine - Cyclic alcohol - Tertiary alcohol - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Lactam - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Hydrocarbon derivative - Organonitrogen compound - Organopnictogen compound - Alcohol - Organooxygen compound - Organic oxide - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as lappaconitine-type diterpenoid alkaloids. These are c18-bisnorditerpenoid alkaloids with a structure based on the heptacyclic lappaconitine skeleton. Lappaconitine similar to aconitane, with the difference that the former lacks a carbon atom at the 18-position.
External Descriptors
Not available