Compound Identification
SMILES
[H][C@]12CCCN1CC1([H])CC2([H])CN2C(=O)CCC[C@@]12[H]
InChIKey
InChIKey=ZALYGVJIPDSPLI-TUUUFIMRSA-N
Formula
C14H22N2O
Mass
234.343
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 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 - Piperidinone - Delta-lactam - N-alkylpyrrolidine - Piperidine - Tertiary carboxylic acid amide - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Lactam - Carboxamide group - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - 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