Compound Identification
SMILES
[O-][N@@+]12CCC[C@@H]1[C@H]1C[C@@H](C2)[C@@H]2CCCC(=O)N2C1
InChIKey
InChIKey=LQWHGNOORGACQX-VGBQHSPPSA-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 Trialkyl amine oxides Tertiary carboxylic acid amides Trisubstituted amine oxides 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 - Trialkyl amine oxide - Tertiary carboxylic acid amide - Pyrrolidine - Lactam - Carboxamide group - Azacycle - Organoheterocyclic compound - Trisubstituted n-oxide - Carboxylic acid derivative - N-oxide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - 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