Compound Identification
SMILES
COC1=C(C)C=C2[C@H]3[C@@H]4N(C)CCC4=CC[C@H]3OC(=O)C2=C1
InChIKey
InChIKey=VVRAKRBGLQJFEA-DJIMGWMZSA-N
Formula
C18H21NO3
Mass
299.37
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 Aralkylamines Alkyl aryl ethers N-alkylpyrrolidines Trialkylamines Lactones Carboxylic acid esters Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Homolycorine skeleton - Benzopyran - Isochromane - 2-benzopyran - Indole or derivatives - Anisole - Phenol ether - Alkyl aryl ether - Aralkylamine - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Lactone - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Ether - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - 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