Compound Identification
SMILES
OC1CCN2CC3CC(CN4C3CCCC4=O)C12
InChIKey
InChIKey=DCXQDHKITGEKSF-UHFFFAOYSA-N
Formula
C14H22N2O2
Mass
250.342
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Lupin alkaloids
- Subclass Leontidine-type alkaloids
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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 Secondary alcohols Amino acids and derivatives 1,2-aminoalcohols 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 - 1,2-aminoalcohol - Amino acid or derivatives - Carboxamide group - Lactam - Tertiary aliphatic amine - Secondary alcohol - Tertiary amine - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Amine - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Carbonyl group - 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