Compound Identification
SMILES
Cl.CCO[C@H]1O[C@@H]2CC=C3CCN(C)[C@H]3[C@@H]2C2=CC(OC)=C(OC)C=C12
InChIKey
InChIKey=JQXCWYYVEHLNPK-MQXQPWMHSA-N
Formula
C20H28ClNO4
Mass
381.9
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 Oxanes N-alkylpyrrolidines Trialkylamines Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Hydrochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Homolycorine skeleton - 2-benzopyran - Isochromane - Benzopyran - Indole or derivatives - Anisole - Alkyl aryl ether - Benzenoid - N-alkylpyrrolidine - Oxane - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Organooxygen 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