Compound Identification
SMILES
O=C1CCCC2C3CC(CN12)C1CCCN1C3
InChIKey
InChIKey=ZALYGVJIPDSPLI-UHFFFAOYSA-N
Formula
C14H22N2O
Mass
234.343
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Lupin alkaloids
- Subclass Leontidine-type alkaloids
-
Class
Lupin alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Lupin alkaloids
Subclass
Leontidine-type alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Leontidine-type alkaloids
Alternative Parents
Quinolizidinones Indolizidines Piperidinones Delta lactams N-alkylpyrrolidines Tertiary carboxylic acid amides Trialkylamines Amino acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Leontidine alkaloid skeleton - Quinolizidinone - Quinolizidine - Indolizidine - Delta-lactam - Piperidinone - Piperidine - N-alkylpyrrolidine - Pyrrolidine - Tertiary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Carboxamide group - Lactam - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Amine - Organopnictogen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organic oxide - Carbonyl group - Hydrocarbon derivative - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as leontidine-type alkaloids. These are lupin alkaloids with a structure based on the leontidine skeleton, a tetracyclic compound containing fused piperidine, pyridine, and pyrrolidine rings.
External Descriptors
Not available