Compound Identification
SMILES
CC(SC1=CC=C(Cl)C=C1)C(=O)OC[C@@H]1CCCN2CCCC[C@H]12
InChIKey
InChIKey=NDXIEKXWGWSJOJ-JGNLYWJMSA-N
Formula
C19H26ClNO2S
Mass
367.93
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Lupin alkaloids
- Subclass Lupinine-type alkaloids
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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 Thiophenol ethers Alkylarylthioethers Chlorobenzenes Piperidines Aryl chlorides Trialkylamines Amino acids and derivatives Carboxylic acid esters Sulfenyl compounds Azacyclic compounds Monocarboxylic acids and derivatives Organochlorides Carbonyl compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Lupinine - Quinolizidine - Quinolizine - Aryl thioether - Thiophenol ether - Halobenzene - Chlorobenzene - Alkylarylthioether - Piperidine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid ester - Amino acid or derivatives - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Monocarboxylic acid or derivatives - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Amine - Carbonyl group - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Aromatic 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
Not available