Compound Identification
SMILES
COC1=C(OC)C=C2C(=O)O[C@@H]3CC=C4CC[N+](C)([O-])[C@H]4[C@@H]3C2=C1
InChIKey
InChIKey=LAEQLQRWNDLBBU-KNFXUPHZSA-N
Formula
C18H21NO5
Mass
331.368
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 N-alkylpyrrolidines Trialkyl amine oxides Lactones Carboxylic acid esters Trisubstituted amine oxides and derivatives Oxacyclic compounds Azacyclic compounds Organic salts Organic oxides Hydrocarbon derivatives Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Homolycorine skeleton - Benzopyran - Isochromane - 2-benzopyran - Indole or derivatives - Anisole - Phenol ether - Alkyl aryl ether - Benzenoid - N-alkylpyrrolidine - Trialkyl amine oxide - Pyrrolidine - Carboxylic acid ester - Lactone - Trisubstituted n-oxide - Organoheterocyclic compound - Azacycle - N-oxide - Oxacycle - Ether - Carboxylic acid derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic salt - Organic cation - 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