Structure Information
Structure

Compound Identification

SMILES

OC1CCN2CC3CC(CN4C3CCCC4=O)C12

InChIKey

InChIKey=DCXQDHKITGEKSF-UHFFFAOYSA-N

Formula

C14H22N2O2

Mass

250.342

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Taxonomic Classification

Taxonomy Tree

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

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

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