Compound Identification
SMILES
COC1=C(OC)C(OC)=C2C(=O)OC3CC=C4CCN(C)C4C3C2=C1C
InChIKey
InChIKey=OZWCYAQHHDNSBD-UHFFFAOYSA-N
Formula
C20H25NO5
Mass
359.422
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 Indoles and derivatives Anisoles Alkyl aryl ethers Aralkylamines N-alkylpyrrolidines Lactones Carboxylic acid esters Trialkylamines Amino acids and derivatives Monocarboxylic acids and derivatives Azacyclic compounds Oxacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Homolycorine skeleton - Benzopyran - Isochromane - 2-benzopyran - Indole or derivatives - Anisole - Alkyl aryl ether - Aralkylamine - N-alkylpyrrolidine - Benzenoid - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Lactone - Carboxylic acid ester - Azacycle - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Ether - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen 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