Compound Identification
SMILES
CN1CCC2CC(OC(C)=O)C3OC(=O)C4=CC5=C(OCO5)C=C4C3C12
InChIKey
InChIKey=LCQDTHLWWZLFDA-UHFFFAOYSA-N
Formula
C19H21NO6
Mass
359.378
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Amaryllidaceae alkaloids
Subclass
Homolycorine-type amaryllidaceae alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Homolycorine-type amaryllidaceae alkaloids
Alternative Parents
2-benzopyrans Benzodioxoles Indoles and derivatives Aralkylamines Benzenoids Dicarboxylic acids and derivatives N-alkylpyrrolidines Carboxylic acid esters Trialkylamines Lactones Amino acids and derivatives Acetals Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organopnictogen compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Homolycorine skeleton - Benzopyran - Isochromane - 2-benzopyran - Benzodioxole - Indole or derivatives - Aralkylamine - Dicarboxylic acid or derivatives - N-alkylpyrrolidine - Benzenoid - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Lactone - Carboxylic acid ester - Azacycle - Oxacycle - Acetal - Organoheterocyclic compound - Carboxylic acid derivative - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as homolycorine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds containing the homolycorine skeleton, made up of a [3,4-g]benzopyranone ring due to the oxidation of the hydroxyl group at the C6. They are biogenetically formed through a restructuring of lycorine-type alkaloids.
External Descriptors
Not available