Compound Identification
SMILES
COC1=C(OC)C=C2[C@H]3[C@H]4C(CC[N+]4(C)[O-])=CC[C@H]3O[C@H](O)C2=C1
InChIKey
InChIKey=PPVYRJCDKXHNEO-OMCOBTAHSA-N
Formula
C18H23NO5
Mass
333.384
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 Hemiacetals Trisubstituted amine oxides and derivatives Oxacyclic compounds Azacyclic compounds Organic zwitterions Organic salts 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 - Benzenoid - N-alkylpyrrolidine - Trialkyl amine oxide - Pyrrolidine - Hemiacetal - Trisubstituted n-oxide - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - N-oxide - Organic salt - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic zwitterion - 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