Compound Identification
SMILES
OCC1CC(CN2CCC(O)CC12)C1CCCC(=O)N1
InChIKey
InChIKey=XFWSJSOEWSRENH-UHFFFAOYSA-N
Formula
C15H26N2O3
Mass
282.384
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Lupin alkaloids
- Subclass Lupinine-type alkaloids
-
Class
Lupin alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Lupin alkaloids
Subclass
Lupinine-type alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Lupinine-type alkaloids
Alternative Parents
Quinolizines Quinolizidines Piperidinones Delta lactams 1,3-aminoalcohols Trialkylamines Secondary carboxylic acid amides Secondary alcohols Amino acids and derivatives Azacyclic compounds Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Lupinine - Quinolizidine - Quinolizine - Delta-lactam - Piperidinone - Piperidine - 1,3-aminoalcohol - Amino acid or derivatives - Carboxamide group - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Amine - Organic nitrogen compound - Carbonyl group - Alcohol - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as lupinine-type alkaloids. These are lupin alkaloids with a structure based on the lupinine skeleton, which is a bicyclic compound consisting of a quinolizidine.
External Descriptors
CHEBI:3289 : quinolizines